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Intensity Pulsed Light Therapy System

EUDAMED

Class IIa (EU MDR)

Ref Intensity Pulsed Light Therapy SystemModel VE2000, VE2000 Pro, VE2000 Pro001, VE2000 Pro002, VE2000 Pro003

by Beijing ADSS Development Co., Ltd

Identity

Trade Name
Intensity Pulsed Light Therapy System EUDAMED
Device Name
Intensity Pulsed Light Therapy System EUDAMED
Model / Reference
VE2000, VE2000 Pro, VE2000 Pro001, VE2000 Pro002, VE2000 Pro003 EUDAMED
Intensity Pulsed Light Therapy System EUDAMED

Identifiers

Primary DI / UDI-DI
06970453271101 EUDAMED
Basic UDI-DI
697045327VE2000BJ EUDAMED
Direct Marketing DI
06970453271101 EUDAMED
EMDN Code
Z12011019 MULTI–PLATFORM LASER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Intensity Pulsed Light Therapy System by Beijing ADSS Development Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000013103
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 1bc256ef-bff6-42ae-bcde-4961895fee20 61 fields · synced Jun 17, 2026