Medical LED Cold Light Source

by Anhui Youtak Medical Technology Co., Ltd. 4 variants

Ref YOUTAK-W662

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697542214YOUTAK-W662001XJ Basic UDI-DI 06975422140099UDI-DI	Date15 Aug 2022Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: YOUTAK-W662

Primary DI / UDI-DI: 06975422140099
Basic UDI-DI: 697542214YOUTAK-W662001XJ
Direct Marketing DI: 06975422140099
EMDN Code: Z12020402 Light sources for endoscopy and minimally invasive surgery

Device Class: Class I
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: CN-MF-000026531
Authorised representative: Kingsmead Service B.V. NL-AR-000002066

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No