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Chambre de trépanation pour iris artificiel

EUDAMED

Class I (EU MDR)

Ref F971AModel Instruments for holding implants during ophthalmic trephination procedures, various designs and sizes

by Fimco

Identity

Trade Name
Chambre de trépanation pour iris artificiel EUDAMED
Device Name
Ophthalmic trephination holding instruments EUDAMED
Model / Reference
Instruments for holding implants during ophthalmic trephination procedures, various designs and sizes EUDAMED
F971A EUDAMED

Identifiers

Primary DI / UDI-DI
03665857005812 EUDAMED
Basic UDI-DI
3665857FAM0904Q4 EUDAMED
EMDN Code
Q020299 CORNEA EXPLANTATION AND TRANSPLANTATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Chambre de trépanation pour iris artificiel by Fimco — 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
Fimco
EUDAMED SRN
FR-MF-000000175

Sources (1)

  • EUDAMED e6a060e9-7a19-4abd-bf6a-d6291c269644 61 fields · synced Sep 18, 2026