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Aramis Trial Insert Ø38 +9

EUDAMED

Class IIa (EU MDR)

Ref EAA IE09Model Orthopaedic prostheses positioners, reusable

by groupe lépine

Identity

Trade Name
ARAMIS TRIAL INSERT Ø38 +9 EUDAMED
Device Name
Orthopaedic prostheses positioners, reusable EUDAMED
Model / Reference
Orthopaedic prostheses positioners, reusable EUDAMED
EAA IE09 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483EAAIE090 EUDAMED
Basic UDI-DI
++M483L091104F9 EUDAMED
Direct Marketing DI
+M483EAAIE090 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 Insert Ø38 +9 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 c7bcee17-a78c-4219-85bf-8e3ac4516a09 61 fields · synced Jun 18, 2026