{"title":"Dermatology Devices \u0026 Clinical Supplies","description":null,"products":[{"product_id":"kernal-kn-4001-uv-phototherapy-cabinet-system-for-vitiligo-and-psoriasis","title":"Kernal KN-4001 UV Phototherapy Cabinet System for Vitiligo and Psoriasis","description":"\u003cp\u003e\u003cstrong\u003eProfessional Whole-Body Phototherapy for Dermatology Institutions\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCertification: FDA 510K cleared\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe KN-4001 is a cabinet-style UV phototherapy system developed for whole-body light treatment in professional dermatology settings. It is positioned for institutions running structured, physician-guided phototherapy programs — including hospital dermatology departments, dedicated phototherapy centers, specialty dermatology clinics, and other skin treatment institutions that need a professionally configured system rather than a spot-treatment device.\u003c\/p\u003e\n\u003cp\u003eThe cabinet format, precision dosing controls, and case management software are built around clinical workflow needs: consistent dosing across sessions, full-body coverage, and documentation of individual patient treatment history.\u003c\/p\u003e\n\u003cp\u003eProduct demo: https:\/\/youtu.be\/Gkdke4NBlTs?si=1VxuQ9id6UgcuZqL\u003c\/p\u003e\n\u003ch2\u003eIndications\u003c\/h2\u003e\n\u003cp\u003eThe KN-4001 is positioned for phototherapy workflows involving:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eVitiligo\u003c\/li\u003e\n\u003cli\u003ePsoriasis\u003c\/li\u003e\n\u003cli\u003eEczema\u003c\/li\u003e\n\u003cli\u003ePityriasis rosea\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTreatment protocols and suitability should be determined by the treating physician based on the specific condition and patient.\u003c\/p\u003e\n\u003ch2\u003eAvailable Configurations\u003c\/h2\u003e\n\u003cp\u003eUnlike the full KN-4001 series (which includes A, A1, and B1 variants at higher lamp wattages), we carry two configurations:\u003c\/p\u003e\n\u003ctable\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth\u003eModel\u003c\/th\u003e\n\u003cth\u003eLamp Configuration\u003c\/th\u003e\n\u003cth\u003eLight Output\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eKN-4001B\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003e40 × 100W UVB lamps\u003c\/td\u003e\n\u003ctd\u003eNarrowband UVB only\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eKN-4001AB\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003e20 × 100W UVA + 20 × 100W UVB lamps\u003c\/td\u003e\n\u003ctd\u003eCombined UVA+UVB output\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003cp\u003e\u003cstrong\u003eChoosing between them:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eKN-4001B\u003c\/strong\u003e is a narrowband UVB-only setup, commonly used for psoriasis and other conditions where NB-UVB is the primary modality.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eKN-4001AB\u003c\/strong\u003e provides simultaneous UVA and UVB output from a shared cabinet, giving institutions flexibility to support PUVA-related and NB-UVB workflows depending on how the treatment protocol is structured, without needing two separate units.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eBoth configurations use the same cabinet body, control system, and touchscreen interface — the difference is strictly in lamp composition and the resulting treatment flexibility.\u003c\/p\u003e\n\u003ch2\u003eLight Source\u003c\/h2\u003e\n\u003cp\u003eBoth models use Philips medical-grade lamps as the light source:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eUVB output:\u003c\/strong\u003e 311nm ±3nm (narrowband)\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eUVA output:\u003c\/strong\u003e 368nm ±3nm (KN-4001AB only)\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eAn internal reflector design is used to maintain high irradiation intensity and shorten treatment time per session.\u003c\/p\u003e\n\u003ch2\u003eKey Features\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eWhole-Body Treatment Cabinet\u003c\/strong\u003e Effective radiation area of approximately 49,000cm² ±10%, with a working distance of 20cm ±1cm — sized for full-body sessions rather than localized treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003ePrecision Dose and Time Control\u003c\/strong\u003e Microcomputer-based control allows treatment to be managed by dose \u003cem\u003eor\u003c\/em\u003e time, with real-time display of equipment working status throughout the session. This supports repeatable, protocol-consistent dosing across visits and across patients.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eIrradiation dose limits: UVA ≤20J\/cm², UVB ≤5J\/cm²\u003c\/li\u003e\n\u003cli\u003eMaximum exposure time: ≤30 minutes per session\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cstrong\u003e8-Inch TFT LCD Touchscreen with Case Management\u003c\/strong\u003e The touchscreen interface includes case management functionality, allowing the system to support recordkeeping per patient. Hardware and software double-monitoring is built in as a safety redundancy layer during treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eOptional UV Intensity Monitoring\u003c\/strong\u003e An optional real-time UV intensity measurement system can be added, allowing the institution to verify actual irradiation output against expected levels — useful for quality assurance and consistent dosing over the lamp's service life.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eVentilation and Cooling System\u003c\/strong\u003e A scientific ventilation and cooling system is built into the cabinet to keep the treatment space comfortable, particularly relevant given sessions can run up to 30 minutes.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eAnti-Interference Technology\u003c\/strong\u003e Proprietary anti-interference technology is built in to maintain normal equipment operation even in environments with strong magnetic fields — relevant for institutions with other electromagnetic equipment nearby (e.g., hospital settings).\u003c\/p\u003e\n\u003ch2\u003eTechnical Specifications\u003c\/h2\u003e\n\u003ctable\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth\u003eSpec\u003c\/th\u003e\n\u003cth\u003eDetail\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003eLamp count\u003c\/td\u003e\n\u003ctd\u003e40 lamps\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eLamp wattage\u003c\/td\u003e\n\u003ctd\u003e100W per lamp\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eEffective radiation area\u003c\/td\u003e\n\u003ctd\u003e49,000cm² ±10%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWorking distance\u003c\/td\u003e\n\u003ctd\u003e20cm ±1cm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eIrradiation dose\u003c\/td\u003e\n\u003ctd\u003eUVA ≤20J\/cm², UVB ≤5J\/cm²\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eOutput wavelength\u003c\/td\u003e\n\u003ctd\u003eUVB: 311nm ±3nm \/ UVA: 368nm ±3nm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eMaximum exposure time\u003c\/td\u003e\n\u003ctd\u003e≤30 minutes\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eDisplay\u003c\/td\u003e\n\u003ctd\u003e8\" TFT LCD touchscreen\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eCertifications\u003c\/td\u003e\n\u003ctd\u003eFDA, ISO13485\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003ch2\u003eFrequently Asked Questions\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eWhat skin conditions is the KN-4001 positioned for?\u003c\/strong\u003e The system is positioned for phototherapy workflows involving vitiligo, psoriasis, eczema, and pityriasis rosea in professional dermatology settings, as directed by the treating physician.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat's the difference between the AB and B models?\u003c\/strong\u003e The B model (KN-4001B) is UVB-only, using all 40 lamps for narrowband UVB output. The AB model (KN-4001AB) splits the 40 lamps into 20 UVA and 20 UVB, allowing combined or independent UVA\/UVB output from one cabinet.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eIs the KN-4001 intended for whole-body treatment?\u003c\/strong\u003e Yes. The cabinet structure and ~49,000cm² radiation area are designed for whole-body phototherapy sessions rather than localized\/handheld treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow is dosing controlled?\u003c\/strong\u003e Via microcomputer control, by dose or by time, with real-time display of equipment status during the session.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDoes it include patient recordkeeping?\u003c\/strong\u003e Yes — the touchscreen includes case management functionality to support per-patient documentation.\u003c\/p\u003e\n\u003chr\u003e\n\u003ch2 dir=\"ltr\"\u003eONE (1) YEAR LIMITED DEPOT WARRANTY \u003c\/h2\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e1. Warranty Provider and Term\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty is provided and administered strictly by the manufacturer of this particular product, not by Medaza, Inc. The manufacturer warrants to the original purchasing entity (\"Buyer\") — including hospitals, clinics, and other licensed medical institutions within the United States — that the hardware product sold shall be free from defects in materials and workmanship under normal clinical use for a period of one (1) year from the date of shipment. This warranty is provided in addition to, and does not affect, any rights the Buyer may hold under applicable state or federal law.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e2. Depot-Only Return Procedure\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eWarranty service is strictly a depot-return process conducted directly by the manufacturer of this particular product.\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eFirst Step (Intake):\u003c\/strong\u003e To initiate a warranty claim, the Buyer must not contact the manufacturer directly. The Buyer must first contact Medaza, Inc. by email at \u003ca href=\"mailto:contactusa@medaza-platform.com\"\u003econtactusa@medaza-platform.com\u003c\/a\u003e.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDelegation:\u003c\/strong\u003e Upon receipt of the email, Medaza, Inc. — acting in its capacity as \u003cstrong\u003edistributor\u003c\/strong\u003e — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated U.S. Initial Importer, where applicable) and the Buyer, facilitating return logistics and securing the required Return Merchandise Authorization (RMA) number.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eShipment:\u003c\/strong\u003e No shipments will be accepted by the manufacturer's facility without an active, authorized RMA number. The product must be securely packaged in its original packaging (or equivalent protective packaging), with all patient-identifying information removed or de-identified in accordance with the Health Insurance Portability and Accountability Act (HIPAA) and other applicable privacy laws prior to shipment, and shipped directly to the designated service facility of the manufacturer.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e3. Allocation of Shipping Costs (Two-Way Shipping)\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe Buyer assumes full financial responsibility for all shipping logistics, packaging, handling fees, customs\/tariffs, and insurance transit costs associated with the warranty claim. This includes:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eInbound Shipping:\u003c\/strong\u003e The cost to safely transport the product from the Buyer's facility to the designated service location of the manufacturer.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOutbound Shipping:\u003c\/strong\u003e The cost to return the repaired or replaced product from the manufacturer's facility back to the Buyer's designated location within the United States.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e4. Recall \u0026amp; Systemic Defect Exception\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe shipping cost allocation in Section 3 shall be waived solely in the event that the returned product is officially determined by the manufacturer, its designated U.S. Initial Importer, Medaza, Inc., or the FDA to be subject to a Recall, Safety Alert, or a verified batch-wide Systemic Manufacturing Defect, in accordance with 21 CFR Part 806 (Medical Device Reporting: Corrections and Removals) and related FDA recall procedures. In such extraordinary circumstances, the manufacturer will cover standard two-way ground shipping costs.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e5. Warranty Exclusions\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty does not cover:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003eDisposable clinical consumables (including but not limited to needles, sutures, applicators, and single-use accessories) once packaging is opened.\u003c\/li\u003e\n\u003cli\u003eDamage caused by accident, abuse, liquid spills, improper sterilization or disinfection, neglect, patient misuse, or unauthorized modifications or repairs.\u003c\/li\u003e\n\u003cli\u003eDamage resulting from use outside the manufacturer's labeled indications, intended use, or instructions for use (IFU).\u003c\/li\u003e\n\u003cli\u003eNormal wear and tear, consumable component degradation (e.g., lamps, filters, probes), or cosmetic degradation that does not affect device function or safety.\u003c\/li\u003e\n\u003cli\u003eAny device on which the serial number, UDI (Unique Device Identifier), or product identification label has been removed, altered, or defaced.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e6. Adverse Event Reporting\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eNothing in this warranty limits or replaces the Buyer's independent obligation, as a healthcare institution or professional user, to report device malfunctions, serious injuries, or adverse events involving this product to the manufacturer, to the manufacturer's designated U.S. Initial Importer (where applicable), to Medaza, Inc. as distributor, and, where required under 21 CFR Part 803 (Medical Device Reporting), to the FDA (e.g., via MedWatch). Medaza, Inc. will cooperate with the manufacturer, the Initial Importer, and the FDA on any resulting investigation, corrective action, or reporting obligation.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e7. Distributor Obligations Notice\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eFor this product, Medaza, Inc. acts solely as a \u003cstrong\u003edistributor\u003c\/strong\u003e; a separate entity — not Medaza, Inc. — handles importation and fulfills any applicable U.S. Initial Importer obligations under FDA regulations for this manufacturer's products. As distributor, Medaza, Inc. confirms it verifies that the device bears the required labeling and UDI, that it is accompanied by the manufacturer's required documentation, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those regulatory obligations, nor does it impose importer obligations on Medaza, Inc.\u003c\/p\u003e","brand":"Kernal","offers":[{"title":"KN-4001B  |\t40 × 100W UVB lamps\tNarrowband UVB only","offer_id":55582189977891,"sku":"KERNAL001-01","price":0.0,"currency_code":"USD","in_stock":true},{"title":"KN-4001A  |20 × 100W UVA + 20 × 100W UVB lamps\tCombined UVA+UVB output","offer_id":55582190010659,"sku":"KERNAL001-02","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0981\/7142\/0963\/files\/69e2b1fba7ec754b738c79f0_screenshot-2026-09-10-at-11.34.25-pm_1789109567440.png?v=1789109904"},{"product_id":"kernel-kn-4003bl2-311nm-narrowband-uvb-lamp-for-vitiligo","title":"Kernel KN-4003BL2 311nm Narrowband UVB Lamp for Vitiligo","description":"\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eCompact, Portable Narrowband UVB Phototherapy Device\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e\u003cmeta charset=\"utf-8\"\u003e \u003cspan\u003eAvailable to beauty clinics and dermatology practices for prescribing to patients as a long-term at-home solution.\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe KN-4003BL2 is a handheld narrowband UVB phototherapy device built around a Philips-manufactured 311nm UV lamp. Designed for portability and ease of use, it is positioned for targeted phototherapy applications where a compact, easy-to-operate device is preferable to a full cabinet system.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eCertification: FDA 510K cleared, CE MDR\u003c\/p\u003e\n\u003ch3 dir=\"ltr\"\u003eIndications\u003c\/h3\u003e\n\u003cp dir=\"ltr\"\u003eThe KN-4003BL2 is positioned for phototherapy workflows involving:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003eVitiligo\u003c\/li\u003e\n\u003cli\u003ePsoriasis\u003c\/li\u003e\n\u003cli\u003eEczema\u003c\/li\u003e\n\u003cli\u003ePityriasis rosea\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003eTreatment protocols and suitability should be determined by the treating physician based on the specific condition and patient.\u003c\/p\u003e\n\u003ch3 dir=\"ltr\"\u003eLight Source\u003c\/h3\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003ePhilips 311nm NB-UVB Lamp\u003c\/strong\u003e\u003cbr\u003eThe device uses a special ultraviolet lamp manufactured by Philips as its treatment light source, selected for high stability and long operating life. The narrowband UVB output is centered at 311nm.\u003c\/p\u003e\n\u003ch3 dir=\"ltr\"\u003eKey Features\u003c\/h3\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eCompact and Portable\u003c\/strong\u003e\u003cbr\u003eSmall in size and easy to carry, the KN-4003BL2 is built for use in settings where portability matters — including travel or business trip use — rather than requiring a fixed cabinet installation.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eSimple, Accessible Operation\u003c\/strong\u003e\u003cbr\u003eStraightforward controls are designed for ease of use.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eDustproof Construction\u003c\/strong\u003e\u003cbr\u003eA dustproof design is built in to support safer, more hygienic treatment sessions.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eTreatment Record Management\u003c\/strong\u003e\u003cbr\u003eThe device supports basic medical record management functionality, helping practitioners quickly establish and look up patient treatment information.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eMicrocomputer Timer Function\u003c\/strong\u003e\u003cbr\u003eA built-in microcomputer timing function tracks and reminds the user of remaining treatment time, removing the need for manual time calculation and helping keep sessions consistent.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eUnique Comb Design\u003c\/strong\u003e\u003cbr\u003eA distinctive comb-style applicator head is built into the device, designed to make treatment application more flexible and convenient — particularly useful for scalp or hair-covered areas.\u003c\/p\u003e\n\u003ch3 dir=\"ltr\"\u003eTechnical Specifications\u003c\/h3\u003e\n\u003cdiv dir=\"ltr\"\u003e\n\u003ctable\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth scope=\"col\"\u003eSpec\u003c\/th\u003e\n\u003cth scope=\"col\"\u003eDetail\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003eBulb\u003c\/td\u003e\n\u003ctd\u003e1 × 9W NB-UVB\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eIrradiation area\u003c\/td\u003e\n\u003ctd\u003e56cm² ± 10%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWorking distance\u003c\/td\u003e\n\u003ctd\u003e3cm ± 0.5cm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eGross weight\u003c\/td\u003e\n\u003ctd\u003e1.5kg\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eSize (L×W×H)\u003c\/td\u003e\n\u003ctd\u003e330mm × 58mm × 46.5mm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWavelength\u003c\/td\u003e\n\u003ctd\u003e311nm (narrowband UVB)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eCertifications\u003c\/td\u003e\n\u003ctd\u003eCE, FDA\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\u003ch3 dir=\"ltr\"\u003eFrequently Asked Questions\u003c\/h3\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eWhat skin conditions is the KN-4003BL2 positioned for?\u003c\/strong\u003e\u003cbr\u003eThe device is positioned for phototherapy workflows involving vitiligo, psoriasis, eczema, and pityriasis rosea, as directed by the treating physician.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eWhat makes this different from the KN-4001 cabinet system?\u003c\/strong\u003e\u003cbr\u003eThe KN-4003BL2 is a compact, portable handheld device suited to targeted or smaller-area treatment, while the KN-4001 is a full cabinet system built for whole-body phototherapy sessions.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eWhat is the comb design used for?\u003c\/strong\u003e\u003cbr\u003eThe comb-style applicator head is designed for more flexible, direct contact application — useful for treating areas like the scalp.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003eHow is treatment time tracked?\u003c\/strong\u003e\u003cbr\u003eA built-in microcomputer timer tracks remaining treatment time and provides reminders during the session.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e \u003c\/p\u003e\n\u003ch2 dir=\"ltr\"\u003eONE (1) YEAR LIMITED DEPOT WARRANTY \u003c\/h2\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e1. Warranty Provider and Term\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty is provided and administered strictly by the manufacturer of this particular product, not by Medaza, Inc. The manufacturer warrants to the original purchasing entity (\"Buyer\") — including hospitals, clinics, and other licensed medical institutions within the United States — that the hardware product sold shall be free from defects in materials and workmanship under normal clinical use for a period of one (1) year from the date of shipment. This warranty is provided in addition to, and does not affect, any rights the Buyer may hold under applicable state or federal law.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e2. Depot-Only Return Procedure\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eWarranty service is strictly a depot-return process conducted directly by the manufacturer of this particular product.\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eFirst Step (Intake):\u003c\/strong\u003e To initiate a warranty claim, the Buyer must not contact the manufacturer directly. The Buyer must first contact Medaza, Inc. by email at \u003ca href=\"mailto:contactusa@medaza-platform.com\"\u003econtactusa@medaza-platform.com\u003c\/a\u003e.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDelegation:\u003c\/strong\u003e Upon receipt of the email, Medaza, Inc. — acting in its capacity as \u003cstrong\u003edistributor\u003c\/strong\u003e — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated U.S. Initial Importer, where applicable) and the Buyer, facilitating return logistics and securing the required Return Merchandise Authorization (RMA) number.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eShipment:\u003c\/strong\u003e No shipments will be accepted by the manufacturer's facility without an active, authorized RMA number. The product must be securely packaged in its original packaging (or equivalent protective packaging), with all patient-identifying information removed or de-identified in accordance with the Health Insurance Portability and Accountability Act (HIPAA) and other applicable privacy laws prior to shipment, and shipped directly to the designated service facility of the manufacturer.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e3. Allocation of Shipping Costs (Two-Way Shipping)\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe Buyer assumes full financial responsibility for all shipping logistics, packaging, handling fees, customs\/tariffs, and insurance transit costs associated with the warranty claim. This includes:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eInbound Shipping:\u003c\/strong\u003e The cost to safely transport the product from the Buyer's facility to the designated service location of the manufacturer.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOutbound Shipping:\u003c\/strong\u003e The cost to return the repaired or replaced product from the manufacturer's facility back to the Buyer's designated location within the United States.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e4. Recall \u0026amp; Systemic Defect Exception\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe shipping cost allocation in Section 3 shall be waived solely in the event that the returned product is officially determined by the manufacturer, its designated U.S. Initial Importer, Medaza, Inc., or the FDA to be subject to a Recall, Safety Alert, or a verified batch-wide Systemic Manufacturing Defect, in accordance with 21 CFR Part 806 (Medical Device Reporting: Corrections and Removals) and related FDA recall procedures. In such extraordinary circumstances, the manufacturer will cover standard two-way ground shipping costs.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e5. Warranty Exclusions\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty does not cover:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003eDisposable clinical consumables (including but not limited to needles, sutures, applicators, and single-use accessories) once packaging is opened.\u003c\/li\u003e\n\u003cli\u003eDamage caused by accident, abuse, liquid spills, improper sterilization or disinfection, neglect, patient misuse, or unauthorized modifications or repairs.\u003c\/li\u003e\n\u003cli\u003eDamage resulting from use outside the manufacturer's labeled indications, intended use, or instructions for use (IFU).\u003c\/li\u003e\n\u003cli\u003eNormal wear and tear, consumable component degradation (e.g., lamps, filters, probes), or cosmetic degradation that does not affect device function or safety.\u003c\/li\u003e\n\u003cli\u003eAny device on which the serial number, UDI (Unique Device Identifier), or product identification label has been removed, altered, or defaced.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e6. Adverse Event Reporting\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eNothing in this warranty limits or replaces the Buyer's independent obligation, as a healthcare institution or professional user, to report device malfunctions, serious injuries, or adverse events involving this product to the manufacturer, to the manufacturer's designated U.S. Initial Importer (where applicable), to Medaza, Inc. as distributor, and, where required under 21 CFR Part 803 (Medical Device Reporting), to the FDA (e.g., via MedWatch). Medaza, Inc. will cooperate with the manufacturer, the Initial Importer, and the FDA on any resulting investigation, corrective action, or reporting obligation.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e7. Distributor Obligations Notice\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eFor this product, Medaza, Inc. acts solely as a \u003cstrong\u003edistributor\u003c\/strong\u003e; a separate entity — not Medaza, Inc. — handles importation and fulfills any applicable U.S. Initial Importer obligations under FDA regulations for this manufacturer's products. As distributor, Medaza, Inc. confirms it verifies that the device bears the required labeling and UDI, that it is accompanied by the manufacturer's required documentation, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those regulatory obligations, nor does it impose importer obligations on Medaza, Inc.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e \u003c\/p\u003e","brand":"Kernal","offers":[{"title":"Default Title","offer_id":55592573272355,"sku":"KERNAL005","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0981\/7142\/0963\/files\/Screenshot2026-09-13at9.22.00PM.png?v=1789361400"},{"product_id":"kernal-kn-4003bl2d-uvb-lamp-light-treatment-for-psoriasis-home-use","title":"Kernal KN-4003BL2D UVB Lamp Light Treatment for Psoriasis","description":"\u003cp\u003e\u003cstrong\u003ePortable Narrowband UVB Phototherapy Device for Home Treatment\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cmeta charset=\"utf-8\"\u003e\n\u003cspan\u003eAvailable to beauty clinics and dermatology practices for prescribing to patients as a long-term at-home solution.\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe KN-4003BL2D is a compact, DC-powered narrowband UVB phototherapy device built around a genuine Philips UV bulb. Designed specifically for ease of use outside a clinical setting, it is positioned for home-use phototherapy under physician guidance, with an optional Bluetooth connection for smartphone app interaction.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCertification: FDA 510K cleared, CE MDR\u003c\/strong\u003e\u003c\/p\u003e\n\u003ch2\u003eIndications\u003c\/h2\u003e\n\u003cp\u003eThe KN-4003BL2D is positioned for phototherapy workflows involving:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eVitiligo\u003c\/li\u003e\n\u003cli\u003ePsoriasis\u003c\/li\u003e\n\u003cli\u003eEczema\u003c\/li\u003e\n\u003cli\u003ePityriasis rosea\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTreatment protocols and suitability should be determined by the treating physician. This device is intended for use as directed by a healthcare provider, including for at-home maintenance phototherapy where clinically appropriate.\u003c\/p\u003e\n\u003ch2\u003eLight Source\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eOriginal Philips UV Bulb\u003c\/strong\u003e The device uses a genuine Philips 9W UV bulb as its light source, selected for high stability and long operating lifespan.\u003c\/p\u003e\n\u003ch2\u003eKey Features\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eDesigned for Home Use\u003c\/strong\u003e Simple, accessible operation is built around at-home treatment, allowing patients to continue phototherapy sessions outside a clinic setting as directed by their physician.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDustproof Protection Cover\u003c\/strong\u003e A dustproof design helps keep treatment safer and supports a longer bulb lifespan.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eOptional Bluetooth \u0026amp; App Connectivity\u003c\/strong\u003e An optional Bluetooth function allows the device to interact with a companion smartphone app, supporting features such as treatment tracking directly from a patient's phone.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDC Power with Rechargeable Battery\u003c\/strong\u003e The device runs on DC power via a rechargeable battery, making it easier to operate without being tethered to an outlet and simple to carry between rooms or while traveling.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eTreatment Record Management\u003c\/strong\u003e Built-in treatment record management supports both physician oversight and patient self-tracking, helping keep a history of sessions over time.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eAdjustable LCD Screen\u003c\/strong\u003e The LCD screen's viewing angle can be adjusted to suit the user's position during treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eTimer Function\u003c\/strong\u003e A built-in timer helps users track session progress and stay within their prescribed treatment time.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eComb Attachment for Scalp Treatment\u003c\/strong\u003e A unique comb-style attachment is included, extending the device's use beyond the face and limbs to scalp treatment — parting hair for more direct light contact.\u003c\/p\u003e\n\u003ch2\u003eTechnical Specifications\u003c\/h2\u003e\n\u003ctable\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth\u003eSpec\u003c\/th\u003e\n\u003cth\u003eDetail\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003eBulb\u003c\/td\u003e\n\u003ctd\u003e1 × 8W UVB bulb (Philips)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eIrradiation area\u003c\/td\u003e\n\u003ctd\u003e56cm² ± 10%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWorking distance\u003c\/td\u003e\n\u003ctd\u003e3cm ± 0.5cm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eGross weight\u003c\/td\u003e\n\u003ctd\u003e1.5kg\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eSize (L×W×H)\u003c\/td\u003e\n\u003ctd\u003e330mm × 58mm × 46.5mm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePower\u003c\/td\u003e\n\u003ctd\u003eDC, rechargeable battery\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eConnectivity\u003c\/td\u003e\n\u003ctd\u003eBluetooth (optional)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eCertifications\u003c\/td\u003e\n\u003ctd\u003eCE, FDA\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003ch2\u003eFrequently Asked Questions\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eIs this device intended for home use?\u003c\/strong\u003e Yes. The KN-4003BL2D is specifically designed for use outside a clinical setting, for patients following a physician-directed home phototherapy plan.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat is the Bluetooth function used for?\u003c\/strong\u003e It's an optional feature that lets the device interact with a companion smartphone app.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat is the comb attachment for?\u003c\/strong\u003e It allows the device to part hair for more direct scalp treatment, in addition to standard use on the face and limbs.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow is the device powered?\u003c\/strong\u003e It runs on DC power via a rechargeable battery rather than requiring a constant wall connection.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow does this compare to the KN-4003BL2?\u003c\/strong\u003e Both are compact, Philips-lamp NB-UVB devices with the same footprint and irradiation specs. The KN-4003BL2D adds DC\/rechargeable battery power and optional Bluetooth app connectivity, positioning it more specifically for home use, while the KN-4003BL2 is described as suited to both home and travel\/business-trip portability.\u003c\/p\u003e\n\u003ch2 dir=\"ltr\"\u003eONE (1) YEAR LIMITED DEPOT WARRANTY \u003c\/h2\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e1. Warranty Provider and Term\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty is provided and administered strictly by the manufacturer of this particular product, not by Medaza, Inc. The manufacturer warrants to the original purchasing entity (\"Buyer\") — including hospitals, clinics, and other licensed medical institutions within the United States — that the hardware product sold shall be free from defects in materials and workmanship under normal clinical use for a period of one (1) year from the date of shipment. This warranty is provided in addition to, and does not affect, any rights the Buyer may hold under applicable state or federal law.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e2. Depot-Only Return Procedure\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eWarranty service is strictly a depot-return process conducted directly by the manufacturer of this particular product.\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eFirst Step (Intake):\u003c\/strong\u003e To initiate a warranty claim, the Buyer must not contact the manufacturer directly. The Buyer must first contact Medaza, Inc. by email at \u003ca href=\"mailto:contactusa@medaza-platform.com\"\u003econtactusa@medaza-platform.com\u003c\/a\u003e.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDelegation:\u003c\/strong\u003e Upon receipt of the email, Medaza, Inc. — acting in its capacity as \u003cstrong\u003edistributor\u003c\/strong\u003e — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated U.S. Initial Importer, where applicable) and the Buyer, facilitating return logistics and securing the required Return Merchandise Authorization (RMA) number.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eShipment:\u003c\/strong\u003e No shipments will be accepted by the manufacturer's facility without an active, authorized RMA number. The product must be securely packaged in its original packaging (or equivalent protective packaging), with all patient-identifying information removed or de-identified in accordance with the Health Insurance Portability and Accountability Act (HIPAA) and other applicable privacy laws prior to shipment, and shipped directly to the designated service facility of the manufacturer.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e3. Allocation of Shipping Costs (Two-Way Shipping)\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe Buyer assumes full financial responsibility for all shipping logistics, packaging, handling fees, customs\/tariffs, and insurance transit costs associated with the warranty claim. This includes:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eInbound Shipping:\u003c\/strong\u003e The cost to safely transport the product from the Buyer's facility to the designated service location of the manufacturer.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOutbound Shipping:\u003c\/strong\u003e The cost to return the repaired or replaced product from the manufacturer's facility back to the Buyer's designated location within the United States.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e4. Recall \u0026amp; Systemic Defect Exception\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe shipping cost allocation in Section 3 shall be waived solely in the event that the returned product is officially determined by the manufacturer, its designated U.S. Initial Importer, Medaza, Inc., or the FDA to be subject to a Recall, Safety Alert, or a verified batch-wide Systemic Manufacturing Defect, in accordance with 21 CFR Part 806 (Medical Device Reporting: Corrections and Removals) and related FDA recall procedures. In such extraordinary circumstances, the manufacturer will cover standard two-way ground shipping costs.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e5. Warranty Exclusions\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty does not cover:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003eDisposable clinical consumables (including but not limited to needles, sutures, applicators, and single-use accessories) once packaging is opened.\u003c\/li\u003e\n\u003cli\u003eDamage caused by accident, abuse, liquid spills, improper sterilization or disinfection, neglect, patient misuse, or unauthorized modifications or repairs.\u003c\/li\u003e\n\u003cli\u003eDamage resulting from use outside the manufacturer's labeled indications, intended use, or instructions for use (IFU).\u003c\/li\u003e\n\u003cli\u003eNormal wear and tear, consumable component degradation (e.g., lamps, filters, probes), or cosmetic degradation that does not affect device function or safety.\u003c\/li\u003e\n\u003cli\u003eAny device on which the serial number, UDI (Unique Device Identifier), or product identification label has been removed, altered, or defaced.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e6. Adverse Event Reporting\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eNothing in this warranty limits or replaces the Buyer's independent obligation, as a healthcare institution or professional user, to report device malfunctions, serious injuries, or adverse events involving this product to the manufacturer, to the manufacturer's designated U.S. Initial Importer (where applicable), to Medaza, Inc. as distributor, and, where required under 21 CFR Part 803 (Medical Device Reporting), to the FDA (e.g., via MedWatch). Medaza, Inc. will cooperate with the manufacturer, the Initial Importer, and the FDA on any resulting investigation, corrective action, or reporting obligation.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e7. Distributor Obligations Notice\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eFor this product, Medaza, Inc. acts solely as a \u003cstrong\u003edistributor\u003c\/strong\u003e; a separate entity — not Medaza, Inc. — handles importation and fulfills any applicable U.S. Initial Importer obligations under FDA regulations for this manufacturer's products. As distributor, Medaza, Inc. confirms it verifies that the device bears the required labeling and UDI, that it is accompanied by the manufacturer's required documentation, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those regulatory obligations, nor does it impose importer obligations on Medaza, Inc.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"Kernal","offers":[{"title":"Default Title","offer_id":55594296475939,"sku":"KERNAL006","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0981\/7142\/0963\/files\/Screenshot2026-09-14at9.36.49AM.png?v=1789404568"},{"product_id":"kernal-kn-4006bl1-311nm-narrowband-uvb-phototherapy-lamp-for-vitiligo","title":"Kernal  KN-4006BL1 311nm Narrowband UVB Phototherapy Lamp for Vitiligo","description":"\u003cp\u003e\u003cstrong\u003eHome-Use Narrowband UVB Phototherapy Device\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cmeta charset=\"utf-8\"\u003e\n\u003cspan\u003eAvailable to beauty clinics and dermatology practices for prescribing to patients as a long-term at-home solution.\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe KN-4006BL1 is a compact narrowband UVB phototherapy device built around a Philips UV lamp light source. Narrowband UVB at 311nm is widely regarded as one of the safest and most effective phototherapy approaches for vitiligo and psoriasis, and the KN-4006BL1 is designed to bring that treatment modality into a simple, home-use format.\u003c\/p\u003e\n\u003ch2\u003eIndications\u003c\/h2\u003e\n\u003cp\u003eThe KN-4006BL1 is positioned for phototherapy workflows involving:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eVitiligo\u003c\/li\u003e\n\u003cli\u003ePsoriasis\u003c\/li\u003e\n\u003cli\u003eEczema\u003c\/li\u003e\n\u003cli\u003eDermatitis\u003c\/li\u003e\n\u003cli\u003ePityriasis rosea\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTreatment protocols and suitability should be determined by the treating physician. This device is intended for use as directed by a healthcare provider, including for at-home maintenance phototherapy where clinically appropriate.\u003c\/p\u003e\n\u003ch2\u003eLight Source\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003ePhilips UV Lamp\u003c\/strong\u003e The device uses a Philips-manufactured UV lamp as its light source, selected for stability and long operating lifespan, providing consistent narrowband UVB output at 311nm across repeated home treatment sessions.\u003c\/p\u003e\n\u003ch2\u003eKey Features\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eRecognized Treatment Approach\u003c\/strong\u003e Narrowband UVB phototherapy is currently recognized as one of the safest and most effective approaches for treating vitiligo and psoriasis, making the KN-4006BL1's format well suited to supporting an established, physician-guided treatment plan.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDust-Proof Design\u003c\/strong\u003e A dust-proof construction is built in to help keep the light source and treatment area protected between uses, supporting safer, more hygienic operation over the device's lifespan.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eSimple, Home-Ready Operation\u003c\/strong\u003e The device is designed for straightforward operation, allowing patients to carry out physician-directed treatment sessions at home rather than requiring a clinic visit for each session — adding convenience for patients managing an ongoing treatment plan.\u003c\/p\u003e\n\u003ch2\u003eCertifications\u003c\/h2\u003e\n\u003cp\u003eCE, FDA\u003c\/p\u003e\n\u003ch2\u003eFrequently Asked Questions\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eWhat skin conditions is the KN-4006BL1 positioned for?\u003c\/strong\u003e The device is positioned for phototherapy workflows involving vitiligo, psoriasis, eczema, dermatitis, and pityriasis rosea, as directed by the treating physician.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eIs this device suitable for home use?\u003c\/strong\u003e Yes. It's designed with simple operation specifically so patients can use it at home as part of a physician-guided treatment plan.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat light source does it use?\u003c\/strong\u003e A Philips UV lamp delivering narrowband UVB output at 311nm.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhy is narrowband UVB used for these conditions?\u003c\/strong\u003e 311nm narrowband UVB is currently recognized as one of the safest and most effective phototherapy wavelengths for treating vitiligo and psoriasis specifically.\u003c\/p\u003e\n\u003ch2 dir=\"ltr\"\u003eONE (1) YEAR LIMITED DEPOT WARRANTY \u003c\/h2\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e1. Warranty Provider and Term\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty is provided and administered strictly by the manufacturer of this particular product, not by Medaza, Inc. The manufacturer warrants to the original purchasing entity (\"Buyer\") — including hospitals, clinics, and other licensed medical institutions within the United States — that the hardware product sold shall be free from defects in materials and workmanship under normal clinical use for a period of one (1) year from the date of shipment. This warranty is provided in addition to, and does not affect, any rights the Buyer may hold under applicable state or federal law.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e2. Depot-Only Return Procedure\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eWarranty service is strictly a depot-return process conducted directly by the manufacturer of this particular product.\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eFirst Step (Intake):\u003c\/strong\u003e To initiate a warranty claim, the Buyer must not contact the manufacturer directly. The Buyer must first contact Medaza, Inc. by email at \u003ca href=\"mailto:contactusa@medaza-platform.com\"\u003econtactusa@medaza-platform.com\u003c\/a\u003e.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDelegation:\u003c\/strong\u003e Upon receipt of the email, Medaza, Inc. — acting in its capacity as \u003cstrong\u003edistributor\u003c\/strong\u003e — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated U.S. Initial Importer, where applicable) and the Buyer, facilitating return logistics and securing the required Return Merchandise Authorization (RMA) number.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eShipment:\u003c\/strong\u003e No shipments will be accepted by the manufacturer's facility without an active, authorized RMA number. The product must be securely packaged in its original packaging (or equivalent protective packaging), with all patient-identifying information removed or de-identified in accordance with the Health Insurance Portability and Accountability Act (HIPAA) and other applicable privacy laws prior to shipment, and shipped directly to the designated service facility of the manufacturer.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e3. Allocation of Shipping Costs (Two-Way Shipping)\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe Buyer assumes full financial responsibility for all shipping logistics, packaging, handling fees, customs\/tariffs, and insurance transit costs associated with the warranty claim. This includes:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eInbound Shipping:\u003c\/strong\u003e The cost to safely transport the product from the Buyer's facility to the designated service location of the manufacturer.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOutbound Shipping:\u003c\/strong\u003e The cost to return the repaired or replaced product from the manufacturer's facility back to the Buyer's designated location within the United States.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e4. Recall \u0026amp; Systemic Defect Exception\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe shipping cost allocation in Section 3 shall be waived solely in the event that the returned product is officially determined by the manufacturer, its designated U.S. Initial Importer, Medaza, Inc., or the FDA to be subject to a Recall, Safety Alert, or a verified batch-wide Systemic Manufacturing Defect, in accordance with 21 CFR Part 806 (Medical Device Reporting: Corrections and Removals) and related FDA recall procedures. In such extraordinary circumstances, the manufacturer will cover standard two-way ground shipping costs.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e5. Warranty Exclusions\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty does not cover:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003eDisposable clinical consumables (including but not limited to needles, sutures, applicators, and single-use accessories) once packaging is opened.\u003c\/li\u003e\n\u003cli\u003eDamage caused by accident, abuse, liquid spills, improper sterilization or disinfection, neglect, patient misuse, or unauthorized modifications or repairs.\u003c\/li\u003e\n\u003cli\u003eDamage resulting from use outside the manufacturer's labeled indications, intended use, or instructions for use (IFU).\u003c\/li\u003e\n\u003cli\u003eNormal wear and tear, consumable component degradation (e.g., lamps, filters, probes), or cosmetic degradation that does not affect device function or safety.\u003c\/li\u003e\n\u003cli\u003eAny device on which the serial number, UDI (Unique Device Identifier), or product identification label has been removed, altered, or defaced.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e6. Adverse Event Reporting\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eNothing in this warranty limits or replaces the Buyer's independent obligation, as a healthcare institution or professional user, to report device malfunctions, serious injuries, or adverse events involving this product to the manufacturer, to the manufacturer's designated U.S. Initial Importer (where applicable), to Medaza, Inc. as distributor, and, where required under 21 CFR Part 803 (Medical Device Reporting), to the FDA (e.g., via MedWatch). Medaza, Inc. will cooperate with the manufacturer, the Initial Importer, and the FDA on any resulting investigation, corrective action, or reporting obligation.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e7. Distributor Obligations Notice\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eFor this product, Medaza, Inc. acts solely as a \u003cstrong\u003edistributor\u003c\/strong\u003e; a separate entity — not Medaza, Inc. — handles importation and fulfills any applicable U.S. Initial Importer obligations under FDA regulations for this manufacturer's products. As distributor, Medaza, Inc. confirms it verifies that the device bears the required labeling and UDI, that it is accompanied by the manufacturer's required documentation, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those regulatory obligations, nor does it impose importer obligations on Medaza, Inc.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"Kernal","offers":[{"title":"Default Title","offer_id":55595530748195,"sku":"KERNAL007","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0981\/7142\/0963\/files\/Screenshot2026-09-14at12.20.29PM.png?v=1789430054"},{"product_id":"kernal-kn-4006bl1d-uvb-light-therapy-phototherapy-lamp","title":"Kernal KN-4006BL1D UVB Light Therapy Phototherapy Lamp","description":"\u003cp\u003e\u003cstrong\u003eHandheld Narrowband UVB Phototherapy Device for Vitiligo and Psoriasis\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cmeta charset=\"utf-8\"\u003e\n\u003cspan\u003eAvailable to beauty clinics and dermatology practices for prescribing to patients as a long-term at-home solution.\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe KN-4006BL1D is a compact, handheld narrowband UVB phototherapy device built around dual Philips medical-grade 311nm UVB lamps. Designed specifically for home use, it combines portability with precision features — proximity sensing, timer control, and optional smartphone connectivity — to support consistent, physician-guided treatment outside a clinical setting.\u003c\/p\u003e\n\u003ch2\u003eIndications\u003c\/h2\u003e\n\u003cp\u003eThe KN-4006BL1D is positioned for phototherapy workflows involving:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eVitiligo\u003c\/li\u003e\n\u003cli\u003ePsoriasis\u003c\/li\u003e\n\u003cli\u003eEczema\u003c\/li\u003e\n\u003cli\u003ePityriasis rosea\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTreatment protocols and suitability should be determined by the treating physician. This device is intended for use as directed by a healthcare provider for at-home phototherapy.\u003c\/p\u003e\n\u003ch2\u003eLight Source\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eDual Philips Medical 311nm NB-UVB Lamps\u003c\/strong\u003e The light source comprises two Philips medical-grade narrowband UVB lamps, delivering high irradiation intensity and efficiency across the treatment area. PUVA or NB-UVB lamp options are available depending on the treatment need.\u003c\/p\u003e\n\u003ch2\u003eKey Features\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eCompact and Portable\u003c\/strong\u003e Small in size and lightweight, the KN-4006BL1D is built for easy carrying, whether moving between rooms at home or bringing the device along while traveling.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHandheld Operation with Flexible Positioning\u003c\/strong\u003e Handheld use allows the treatment site to be targeted flexibly, rather than being limited to a fixed treatment position.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eAcrylic Protective Shield\u003c\/strong\u003e A dust-proof design is paired with an acrylic shield made from special optical materials, providing enhanced protection during treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eTimer and Time Working Mode\u003c\/strong\u003e A built-in timer function and time-based working mode improve treatment accuracy and safety by removing the need for manual time calculation, with a countdown display to help patients track session progress in real time.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eInternal Lithium-Ion Battery\u003c\/strong\u003e Powered by a replaceable lithium-ion battery, the device can be operated cord-free, adding convenience for home use without being tied to a power outlet during treatment.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eProximity Sensor with Positioning Bracket\u003c\/strong\u003e A proximity sensor paired with a positioning bracket helps users quickly and accurately locate the correct working distance, supporting more precise, consistent treatment sessions.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eSmart Treatment via Bluetooth (Optional)\u003c\/strong\u003e An optional Bluetooth function allows the device to connect with a companion smartphone app, offering complimentary treatment consultation support alongside home use.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCase Management\u003c\/strong\u003e Built-in case management functionality supports efficient medical record keeping, allowing for swift retrieval of patient treatment information — useful for both patient self-tracking and physician review.\u003c\/p\u003e\n\u003ch2\u003eTechnical Specifications\u003c\/h2\u003e\n\u003ctable\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth\u003eSpec\u003c\/th\u003e\n\u003cth\u003eDetail\u003c\/th\u003e\n\u003c\/tr\u003e\n\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003eLight source\u003c\/td\u003e\n\u003ctd\u003e2 × Philips medical 311nm NB-UVB lamps\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eIrradiation intensity\u003c\/td\u003e\n\u003ctd\u003e7mW\/cm²\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWorking distance\u003c\/td\u003e\n\u003ctd\u003e3cm ± 0.5cm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eOutput wavelength range\u003c\/td\u003e\n\u003ctd\u003e311–312nm\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eMaximum exposure time\u003c\/td\u003e\n\u003ctd\u003e≤30 minutes\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eSafety classification\u003c\/td\u003e\n\u003ctd\u003eType II, Internal Power\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePower supply\u003c\/td\u003e\n\u003ctd\u003eReplaceable lithium-ion battery\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eCertifications\u003c\/td\u003e\n\u003ctd\u003eCE, FDA\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003ch2\u003eFrequently Asked Questions\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eIs this device suitable for home use?\u003c\/strong\u003e Yes — it's specifically designed for home treatment, with simple, user-friendly operation and case management to support ongoing physician-guided care.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow is treatment distance managed?\u003c\/strong\u003e A proximity sensor and positioning bracket help users quickly locate and maintain the correct working distance for accurate, consistent sessions.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat is the Bluetooth function used for?\u003c\/strong\u003e It's an optional feature connecting the device to a companion smartphone app for treatment consultation support.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow long can a single session run?\u003c\/strong\u003e Maximum exposure time is capped at 30 minutes per the device's safety parameters.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow does this compare to the KN-4006BL1?\u003c\/strong\u003e The KN-4006BL1D is the more feature-rich handheld variant — dual lamps, battery power, proximity sensing, and optional Bluetooth\/app connectivity — built specifically for home use, while the KN-4006BL1 is positioned more simply around ease of home operation with a single Philips lamp light source.\u003c\/p\u003e\n\u003ch2 dir=\"ltr\"\u003eONE (1) YEAR LIMITED DEPOT WARRANTY \u003c\/h2\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e1. Warranty Provider and Term\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty is provided and administered strictly by the manufacturer of this particular product, not by Medaza, Inc. The manufacturer warrants to the original purchasing entity (\"Buyer\") — including hospitals, clinics, and other licensed medical institutions within the United States — that the hardware product sold shall be free from defects in materials and workmanship under normal clinical use for a period of one (1) year from the date of shipment. This warranty is provided in addition to, and does not affect, any rights the Buyer may hold under applicable state or federal law.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e2. Depot-Only Return Procedure\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eWarranty service is strictly a depot-return process conducted directly by the manufacturer of this particular product.\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eFirst Step (Intake):\u003c\/strong\u003e To initiate a warranty claim, the Buyer must not contact the manufacturer directly. The Buyer must first contact Medaza, Inc. by email at \u003ca href=\"mailto:contactusa@medaza-platform.com\"\u003econtactusa@medaza-platform.com\u003c\/a\u003e.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDelegation:\u003c\/strong\u003e Upon receipt of the email, Medaza, Inc. — acting in its capacity as \u003cstrong\u003edistributor\u003c\/strong\u003e — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated U.S. Initial Importer, where applicable) and the Buyer, facilitating return logistics and securing the required Return Merchandise Authorization (RMA) number.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eShipment:\u003c\/strong\u003e No shipments will be accepted by the manufacturer's facility without an active, authorized RMA number. The product must be securely packaged in its original packaging (or equivalent protective packaging), with all patient-identifying information removed or de-identified in accordance with the Health Insurance Portability and Accountability Act (HIPAA) and other applicable privacy laws prior to shipment, and shipped directly to the designated service facility of the manufacturer.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e3. Allocation of Shipping Costs (Two-Way Shipping)\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe Buyer assumes full financial responsibility for all shipping logistics, packaging, handling fees, customs\/tariffs, and insurance transit costs associated with the warranty claim. This includes:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003e\n\u003cstrong\u003eInbound Shipping:\u003c\/strong\u003e The cost to safely transport the product from the Buyer's facility to the designated service location of the manufacturer.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOutbound Shipping:\u003c\/strong\u003e The cost to return the repaired or replaced product from the manufacturer's facility back to the Buyer's designated location within the United States.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e4. Recall \u0026amp; Systemic Defect Exception\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThe shipping cost allocation in Section 3 shall be waived solely in the event that the returned product is officially determined by the manufacturer, its designated U.S. Initial Importer, Medaza, Inc., or the FDA to be subject to a Recall, Safety Alert, or a verified batch-wide Systemic Manufacturing Defect, in accordance with 21 CFR Part 806 (Medical Device Reporting: Corrections and Removals) and related FDA recall procedures. In such extraordinary circumstances, the manufacturer will cover standard two-way ground shipping costs.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e5. Warranty Exclusions\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eThis warranty does not cover:\u003c\/p\u003e\n\u003cul dir=\"ltr\"\u003e\n\u003cli\u003eDisposable clinical consumables (including but not limited to needles, sutures, applicators, and single-use accessories) once packaging is opened.\u003c\/li\u003e\n\u003cli\u003eDamage caused by accident, abuse, liquid spills, improper sterilization or disinfection, neglect, patient misuse, or unauthorized modifications or repairs.\u003c\/li\u003e\n\u003cli\u003eDamage resulting from use outside the manufacturer's labeled indications, intended use, or instructions for use (IFU).\u003c\/li\u003e\n\u003cli\u003eNormal wear and tear, consumable component degradation (e.g., lamps, filters, probes), or cosmetic degradation that does not affect device function or safety.\u003c\/li\u003e\n\u003cli\u003eAny device on which the serial number, UDI (Unique Device Identifier), or product identification label has been removed, altered, or defaced.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e6. Adverse Event Reporting\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eNothing in this warranty limits or replaces the Buyer's independent obligation, as a healthcare institution or professional user, to report device malfunctions, serious injuries, or adverse events involving this product to the manufacturer, to the manufacturer's designated U.S. Initial Importer (where applicable), to Medaza, Inc. as distributor, and, where required under 21 CFR Part 803 (Medical Device Reporting), to the FDA (e.g., via MedWatch). Medaza, Inc. will cooperate with the manufacturer, the Initial Importer, and the FDA on any resulting investigation, corrective action, or reporting obligation.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e7. Distributor Obligations Notice\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eFor this product, Medaza, Inc. acts solely as a \u003cstrong\u003edistributor\u003c\/strong\u003e; a separate entity — not Medaza, Inc. — handles importation and fulfills any applicable U.S. Initial Importer obligations under FDA regulations for this manufacturer's products. As distributor, Medaza, Inc. confirms it verifies that the device bears the required labeling and UDI, that it is accompanied by the manufacturer's required documentation, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those regulatory obligations, nor does it impose importer obligations on Medaza, Inc.\u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003e \u003c\/p\u003e","brand":"Improve Medical USA","offers":[{"title":"Default Title","offer_id":55595671388451,"sku":"KERNAL008","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0981\/7142\/0963\/files\/Screenshot2026-09-14at5.08.11PM.png?v=1789431384"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0981\/7142\/0963\/collections\/Screenshot_2026-09-11_at_12.52.35_AM.png?v=1789113367","url":"https:\/\/us.medaza-platform.com\/collections\/dermatology-devices-clinical-supplies.oembed","provider":"Medaza, Inc. (USA)","version":"1.0","type":"link"}