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Aramis Baseplate Impactor Ø28

EUDAMED

Class I (EU MDR)

Ref EAA GI00Model Class Ir Instrument

by groupe lépine

Identity

Trade Name
ARAMIS BASEPLATE IMPACTOR Ø28 EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
EAA GI00 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483EAAGI000 EUDAMED
Basic UDI-DI
++M483L0911YN EUDAMED
Direct Marketing DI
+M483EAAGI000 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER 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

Aramis Baseplate Impactor Ø28 by groupe lépine — 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
groupe lépine
EUDAMED SRN
FR-MF-000001182

Sources (1)

  • EUDAMED cfca567f-aee7-4f09-ba87-2af0c59dbf45 61 fields · synced Jun 18, 2026