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Plastic Full Rim

EUDAMED

Class I (EU MDR)

Ref R26395-0

by Wenzhou Sense Optical Co., Ltd.

Identity

Device Name
Plastic Full Rim EUDAMED
Model / Reference
R26395-0 EUDAMED

Identifiers

Primary DI / UDI-DI
06974600430519 EUDAMED
Basic UDI-DI
697460043FFPPZ EUDAMED
EMDN Code
Q02100202 PLASTIC SPECTACLE FRAMES WITHOUT LENSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Plastic Full Rim by Wenzhou Sense Optical Co., Ltd. — Class I — 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-000009540
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 533c4f39-16d9-42d7-b091-a61d3f730449 61 fields · synced Jun 18, 2026