{"product_id":"kn-5000d-308nm-excimer-laser-system-targeted-dermatology-treatment-for-vitiligo","title":"Kernal KN-5000D 308nm Excimer Laser System — Targeted Dermatology Treatment for Vitiligo","description":"\u003cp\u003e\u003cstrong\u003eCompact, High-Precision 308nm Excimer Phototherapy for Clinical and Home Settings\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe KN-5000D is a compact 308nm excimer laser phototherapy system built around imported xenon chloride (XeCl) excimer light source technology. Designed with a smaller footprint and lower consumable cost than larger excimer platforms, it delivers high-intensity, precisely targeted treatment suitable for both clinical dermatology settings and stationary home use.\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-5000D 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 lesion size, location, and patient condition.\u003c\/p\u003e\n\u003ch2\u003eLight Source\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eXeCl Excimer Light — 308nm\u003c\/strong\u003e The system uses the latest generation of imported xenon chloride gas light source, continuously emitting high-intensity single-frequency 308nm excimer light with a stable waveband and pure spot — supporting effective, targeted treatment with fewer sessions than lower-intensity phototherapy approaches.\u003c\/p\u003e\n\u003ch2\u003eKey Features\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eCompact, Cost-Efficient Design\u003c\/strong\u003e A smaller footprint and lower consumable cost make the KN-5000D a more accessible entry point into excimer phototherapy, without sacrificing output intensity.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eQuick Start, Simple Operation\u003c\/strong\u003e The system is designed for quick startup and straightforward day-to-day operation, minimizing setup time between patients or sessions.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHigh-Precision Targeting\u003c\/strong\u003e Good targeting accuracy allows the system to treat lesions with minimal impact on surrounding healthy skin, including lesions in areas traditional light-based devices have difficulty reaching effectively.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eSix Multi-Spec Shading Sheets\u003c\/strong\u003e Six different sizes of shading sheets are included, allowing precise control over the irradiation range so treatment can be matched to different lesion sizes.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eAutomatic MED (Minimal Erythema Dose) Testing\u003c\/strong\u003e A built-in UV dosage scheme enables automatic six-spot skin phototoxicity testing, simplifying dose calibration into an easy, patient-specific process rather than a manual, time-consuming one.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDual Treatment Modes\u003c\/strong\u003e Both dose mode and time mode are available, giving practitioners flexibility to select the treatment approach that best fits the protocol.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e8\" Touch Screen with GUI\u003c\/strong\u003e An 8-inch touch screen paired with a user-friendly GUI is designed to make operation easier and safer to monitor throughout a session.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eFingerprint Management System\u003c\/strong\u003e A fingerprint-based management system allows treatment records for different users or patients to be collected and retrieved quickly — useful for multi-patient clinical settings as well as tracking an individual's home treatment history.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eIrradiation Intensity Calibration\u003c\/strong\u003e A built-in calibration system helps ensure accurate, consistent treatment dosage is maintained over time.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eOptional Mobile Trolley\u003c\/strong\u003e An optional flexible trolley is available, making the device easier to move within a dermatology clinic or hospital setting to meet different workflow needs.\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\u003e308nm excimer light (XeCl)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eSpot size\u003c\/td\u003e\n\u003ctd\u003e20cm² ± 10%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eIrradiation intensity\u003c\/td\u003e\n\u003ctd\u003e50 mW\/cm² ± 10%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eLight source lifespan\u003c\/td\u003e\n\u003ctd\u003e≥500 hours\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWeight\u003c\/td\u003e\n\u003ctd\u003e12kg (gross weight)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePower supply\u003c\/td\u003e\n\u003ctd\u003eAC100–240V, 50\/60Hz\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eDisplay\u003c\/td\u003e\n\u003ctd\u003e8\" touch screen\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eCertifications\u003c\/td\u003e\n\u003ctd\u003eCE, FDA, ISO13485, CFDA\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003ch2\u003eWho It's For\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eDermatology clinics\u003c\/li\u003e\n\u003cli\u003eHospital dermatology departments\u003c\/li\u003e\n\u003cli\u003eSpecialty phototherapy centers\u003c\/li\u003e\n\u003cli\u003eStationary home-use settings, under physician guidance\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003eFrequently Asked Questions\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eWhat makes the KN-5000D different from the KN-5000C?\u003c\/strong\u003e Both use the same 308nm XeCl excimer light source and 50 mW\/cm² intensity. The KN-5000D is positioned as a more compact, lower-consumable-cost platform with fingerprint-based patient management, suitable for both clinical and stationary home use, while the KN-5000C is built around a flexible handheld treatment head with quick-connect light source replacement for higher-throughput clinical settings.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eIs this device suitable for home use?\u003c\/strong\u003e Yes — the KN-5000D's stationary design is described as suitable for both clinical and home use, under a physician-directed treatment plan.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat is the fingerprint management system used for?\u003c\/strong\u003e It allows treatment records for multiple users or patients to be collected and retrieved quickly, supporting recordkeeping in both multi-patient clinical settings and individual home tracking.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eHow does MED testing work on this device?\u003c\/strong\u003e The system automates a six-spot phototoxicity test to determine the correct UV dose for the patient's specific skin characteristics, simplifying what would otherwise be a complex manual process.\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":48371853820091,"sku":"KERNAL010","price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0718\/9040\/3515\/files\/Screenshot2026-09-16at3.40.24PM.png?v=1789599942","url":"https:\/\/eu.medaza-platform.com\/products\/kn-5000d-308nm-excimer-laser-system-targeted-dermatology-treatment-for-vitiligo","provider":"Medaza Europe ","version":"1.0","type":"link"}