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Aramis Trial Glenoid Ø36mm R34

EUDAMED

Class IIa (EU MDR)

Ref EAA GE00Model Orthopaedic prostheses positioners, reusable

by groupe lépine

Identity

Trade Name
ARAMIS TRIAL GLENOID Ø36MM R34 EUDAMED
Device Name
Orthopaedic prostheses positioners, reusable EUDAMED
Model / Reference
Orthopaedic prostheses positioners, reusable EUDAMED
EAA GE00 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483EAAGE000 EUDAMED
Basic UDI-DI
++M483L091104F9 EUDAMED
Direct Marketing DI
+M483EAAGE000 EUDAMED
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED

Classification

Device Class
Class IIa 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

Aramis Trial Glenoid Ø36mm R34 by groupe lépine — Class IIa — 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 490f4a50-7e5b-4834-adc0-fde3c0a71d4c 61 fields · synced Jul 15, 2026