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Goldfinger Alignment Rod N°2

EUDAMED

Class I (EU MDR)

Ref GL2900-016Model Class Ir Instrument

by groupe lépine

Identity

Trade Name
GOLDFINGER ALIGNMENT ROD N°2 EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
GL2900-016 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483GL29000160 EUDAMED
Basic UDI-DI
++M483L0911YN EUDAMED
Direct Marketing DI
+M483GL29000160 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

Goldfinger Alignment Rod N°2 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 2b16ba63-3481-420b-b5d4-d5daa3472be3 61 fields · synced Jun 19, 2026