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OPHTHALMIC FORCEPS(Model:capsulorhexis forceps)

EUDAMED

Class I (EU MDR)

Ref 23-CP001024Ref 23-CP001004

by Gaush Precision Ltd

Identity

Trade Name
OPHTHALMIC FORCEPS(Model:capsulorhexis forceps) EUDAMED
OPHTHALMIC FORCEPS(Model: capsulorhexis forceps) EUDAMED
Device Name
OPHTHALMIC FORCEPS EUDAMED
Model / Reference
23-CP001024 EUDAMED
23-CP001004 EUDAMED

Identifiers

Primary DI / UDI-DI
06974957360378 EUDAMED
06974957360316 EUDAMED
Basic UDI-DI
697495736ED001K9 EUDAMED
EMDN Code
Q021102 OPHTHALMIC SURGERY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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(Model:capsulorhexis forceps) 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 (2)

  • EUDAMED 9ae7d8db-4ce2-43f3-aecd-068845da702e 61 fields · synced Jul 16, 2026
  • EUDAMED 6f58aeaf-9d78-4e34-a425-0b26e833ea8a 61 fields · synced May 18, 2026