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S51002

EUDAMED

Class IIa (EU MDR)

Ref S51002

by Ophmed Co., Ltd.

Identity

Device Name
Disposable Ophthalmic Forceps EUDAMED
Model / Reference
S51002 EUDAMED

Identifiers

Primary DI / UDI-DI
06974482530079 EUDAMED
Basic UDI-DI
B-06974482530079 EUDAMED
697448253S110009U EUDAMED
EMDN Code
Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

S51002 by Ophmed Co., Ltd. — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ophmed Co., Ltd.
EUDAMED SRN
CN-MF-000032262
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (2)

  • EUDAMED c0c44b2b-bcfb-4ea9-82eb-b3ed614fc2b6 61 fields · synced Jun 18, 2026
  • EUDAMED f2d3c0fa-71d2-403e-8e13-4f007d1c89c0 61 fields · synced May 17, 2026