{"product_id":"kernal-led-photodynamic-light-therapy-machine-kn-7000d","title":"Kernal KN-7000D LED Photodynamic Light Therapy Machine","description":"\u003ch1\u003eKN-7000D LED Photodynamic Light Therapy Machine\u003c\/h1\u003e\n\u003cp\u003e\u003cbr\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eProfessional Multi-Color LED Light Therapy for Acne, Inflammation, and Wound Healing\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cmeta charset=\"utf-8\"\u003eAvailable across all EU countries except Germany\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe KN-7000D is a professional LED photodynamic light therapy system designed for structured, non-invasive skin treatment in clinical settings. Built around a high-power SMD matrix light source with red, blue, and yellow output, the KN-7000D is positioned for institutions running acne care, inflammation management, and post-procedure wound healing protocols.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCertification\u003c\/strong\u003e: CE MDR\u003c\/p\u003e\n\u003ch2\u003eIndications\u003c\/h2\u003e\n\u003cp\u003eThe KN-7000D is positioned for:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eInflammatory acne\u003c\/li\u003e\n\u003cli\u003eInflammation elimination\u003c\/li\u003e\n\u003cli\u003ePromotion of skin wound healing\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTreatment selection and protocol should be determined by the treating practitioner based on the patient's condition.\u003c\/p\u003e\n\u003ch2\u003eLight Source \u0026amp; Color Combination\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eHigh-Power SMD Matrix Light Source\u003c\/strong\u003e A densely arranged SMD matrix light source boosts irradiation intensity while maintaining a uniform light spot across the treatment area — designed to avoid the \"hot spots\" or uneven output that can come with lower-density LED arrangements.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eMulti-Color Combination\u003c\/strong\u003e The treatment head supports red, blue, and yellow light, selectable as single-color or combined three-color output from one head. This allows practitioners to match the light source configuration to the specific clinical requirement, rather than switching devices between treatment types.\u003c\/p\u003e\n\u003ch2\u003eKey Features\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eDose Working Mode with Intensity Calibration\u003c\/strong\u003e A dedicated dose mode, paired with a radiation intensity calibration system, is built in to help ensure treatment precision session to session — supporting more consistent, repeatable dosing rather than relying on fixed time settings alone.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e5 Pre-Stored Treatment Plans\u003c\/strong\u003e Five pre-stored treatment plans are built in, with one-click selection designed to simplify day-to-day operation for clinical staff.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eContinuous and Pulse Irradiation Modes\u003c\/strong\u003e Two working modes — continuous and pulse irradiation — give practitioners more flexibility to match treatment delivery to different clinical needs.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eAdjustable, Extendable Treatment Head\u003c\/strong\u003e The treatment head is adjustable to accommodate various treatment areas. An aerodynamic design combined with high-grade thermal materials is intended to keep the head stable and safe to operate, even during extended clinical use.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCantilever Positioning\u003c\/strong\u003e A cantilever design allows the light panel to be fixed at any desired angle or position, supporting easier positioning across different treatment areas and patient setups.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e8\" Full Touch Screen\u003c\/strong\u003e An 8-inch full touch screen with a user-friendly GUI is designed to make operation more concise and smooth for clinical staff.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003ePatient Comfort Features\u003c\/strong\u003e A warm voice reminder function is included to support a more relaxed, comfortable treatment experience for patients during sessions.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDual-Layer Access Protection\u003c\/strong\u003e A key switch combined with a power-on password provides two layers of protection against unauthorized or unrelated use of the device.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eNon-Invasive, High-Purity Light Source\u003c\/strong\u003e The system uses a high-purity light source for non-invasive treatment, with no special aftercare required following a session.\u003c\/p\u003e\n\u003ch2\u003eTechnical Overview\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\u003eHigh-power SMD matrix LED\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eColor options\u003c\/td\u003e\n\u003ctd\u003eRed, Blue, Yellow (single or 3-color combination)\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWorking modes\u003c\/td\u003e\n\u003ctd\u003eContinuous \/ Pulse\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eTreatment plans\u003c\/td\u003e\n\u003ctd\u003e5 pre-stored plans\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eDisplay\u003c\/td\u003e\n\u003ctd\u003e8\" full touch screen\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eAccess control\u003c\/td\u003e\n\u003ctd\u003eKey switch + power-on password\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eCertifications\u003c\/td\u003e\n\u003ctd\u003eISO13485, CFDA, CE\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\u003eMedical aesthetics practices\u003c\/li\u003e\n\u003cli\u003eSkin treatment centers\u003c\/li\u003e\n\u003c\/ul\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\u003cbr\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":48357939413179,"sku":"KERNAL003","price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0718\/9040\/3515\/files\/Screenshot2026-09-13at6.50.52PM.png?v=1789350802","url":"https:\/\/eu.medaza-platform.com\/products\/kernal-led-photodynamic-light-therapy-machine-kn-7000d","provider":"Medaza Europe ","version":"1.0","type":"link"}