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0030

EUDAMED

Class I (EU MDR)

Ref 030

by Wenzhou Tide-Optical Co., Ltd

Identity

Device Name
0030 EUDAMED
Model / Reference
030 EUDAMED

Identifiers

Primary DI / UDI-DI
06974213560016 EUDAMED
Basic UDI-DI
69742135600307L EUDAMED
EMDN Code
Q02100299 SPECTACLE FRAMES WITHOUT LENSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

Yes

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

0030 by Wenzhou Tide-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-000009512
Authorised Representative
Share Info Consultant Service LLC Repräsentanzbüro DE-AR-000005133

Sources (1)

  • EUDAMED a5e2820f-5848-4165-b252-5fdc076cbd61 61 fields · synced Jul 12, 2026