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Aramis Insert Impactor Ø38

EUDAMED

Class I (EU MDR)

Ref EAA EIISModel Class Ir Instrument

by groupe lépine

Identity

Trade Name
ARAMIS INSERT IMPACTOR Ø38 EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
EAA EIIS EUDAMED

Identifiers

Primary DI / UDI-DI
+M483EAAEIIS0 EUDAMED
Basic UDI-DI
++M483L0911YN EUDAMED
Direct Marketing DI
+M483EAAEIIS0 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 Insert Impactor Ø38 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 3c59ea61-13f6-4b49-b403-cb51de8e4c32 61 fields · synced Jul 14, 2026