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Tibial Guide Ring

EUDAMED

Class I (EU MDR)

Ref GKAGB001Model Class Ir Instrument

by groupe lépine

Identity

Trade Name
TIBIAL GUIDE RING EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
GKAGB001 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483GKAGB0010 EUDAMED
Basic UDI-DI
++M483L0911YN EUDAMED
Direct Marketing DI
+M483GKAGB0010 EUDAMED
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Orthopaedic implant impactor, reusable

Tibial Guide Ring by groupe lépine — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
groupe lépine
EUDAMED SRN
FR-MF-000001182

Sources (1)

  • EUDAMED 5354fe34-4720-4923-ae0b-bea0c15cb8cc 61 fields · synced Jun 18, 2026