{"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\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\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003ch2 dir=\"ltr\"\u003eONE (1) YEAR LIMITED DEPOT WARRANTY (EU\/EEA — CE MDR Version)\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 Europe, d.o.o. The manufacturer warrants to the original purchasing entity (\"Buyer\") — including hospitals, clinics, and other licensed medical institutions within the European Union \/ European Economic Area — 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 statutory rights the Buyer may hold as a matter of applicable EU or national consumer or commercial 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 Europe, d.o.o. by email at \u003ca href=\"mailto:contacteurope2@medaza-platform.com\"\u003econtacteurope2@medaza-platform.com\u003c\/a\u003e.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDelegation:\u003c\/strong\u003e Upon receipt of the email, Medaza Europe, d.o.o. — acting in its capacity as \u003cstrong\u003edistributor\u003c\/strong\u003e under Regulation (EU) 2017\/745 (the Medical Device Regulation, \"MDR\") — will delegate and coordinate the direct connection between the manufacturer (or the manufacturer's designated EU importer of record) 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 Regulation (EU) 2016\/679 (the General Data Protection Regulation, \"GDPR\") and applicable national data protection requirements 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 EU\/EEA.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e4. Field Safety Corrective Action \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 EU importer of record, Medaza Europe, d.o.o., or an authorized regulatory body (e.g., a national Competent Authority such as JAZMP, or another EU\/EEA Competent Authority) to be subject to a \u003cstrong\u003eField Safety Corrective Action (FSCA)\u003c\/strong\u003e, Field Safety Notice, or a verified batch-wide Systemic Manufacturing Defect, in accordance with the vigilance and market surveillance requirements of MDR Articles 87–92. 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 purpose, or instructions for use (IFU), as defined under MDR Article 2.\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 Unique Device Identifier (UDI), serial number, or product identification label has been removed, altered, or defaced.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp dir=\"ltr\"\u003e\u003cstrong\u003e6. Incident Reporting and Vigilance\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 serious incidents or field safety issues involving this product in accordance with MDR Article 87. Reports should be directed to the manufacturer, to the manufacturer's designated EU importer of record, to Medaza Europe, d.o.o. as distributor, and, where required, to the relevant national Competent Authority (e.g., JAZMP) and\/or logged via EUDAMED once the relevant EUDAMED modules become mandatory. Medaza Europe, d.o.o. will cooperate with the manufacturer, the importer of record, and Competent Authorities on any resulting vigilance 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\u003e \u003c\/p\u003e\n\u003cp dir=\"ltr\"\u003eFor this product, Medaza Europe, d.o.o. acts solely as \u003cstrong\u003edistributor\u003c\/strong\u003e under MDR Article 14; a separate, designated importer of record — not Medaza Europe, d.o.o. — fulfills the importer obligations under MDR Article 13 for this manufacturer's products. As distributor, Medaza Europe, d.o.o. confirms it verifies that the device bears the required CE marking and UDI, that it is accompanied by the manufacturer's required documentation and, where applicable, the importer's required labeling, and that appropriate storage and transport conditions are maintained while the product is under its responsibility. This warranty does not alter or diminish those statutory obligations, nor does it impose importer obligations on Medaza Europe, d.o.o.\u003c\/p\u003e","brand":"Kernal Medical","offers":[{"title":"Default Title","offer_id":48360883159227,"sku":"KERNAL006","price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0718\/9040\/3515\/files\/Screenshot2026-09-14at9.36.49AM.png?v=1789403907","url":"https:\/\/eu.medaza-platform.com\/products\/kernal-kn-4003bl2d-uvb-lamp-light-treatment-for-psoriasis-home-use","provider":"Medaza Europe ","version":"1.0","type":"link"}