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OPHTHALMIC FORCEPS(needle holder)

EUDAMED

Class I (EU MDR)

Ref 23-CP005005

by Gaush Precision Ltd

Identity

Trade Name
OPHTHALMIC FORCEPS(needle holder) EUDAMED
Device Name
OPHTHALMIC FORCEPS EUDAMED
Model / Reference
23-CP005005 EUDAMED

Identifiers

Primary DI / UDI-DI
06974957360743 EUDAMED
Basic UDI-DI
697495736ED001K9 EUDAMED
EMDN Code
Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

OPHTHALMIC FORCEPS(needle holder) by Gaush Precision 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

Manufacturer
Gaush Precision Ltd
EUDAMED SRN
CN-MF-000028969
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED f1319da0-5b6c-458f-9425-af3baa421dae 61 fields · synced Jun 19, 2026