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Aramis Stem Impactor

EUDAMED

Class I (EU MDR)

Ref ETA IMPTModel Class Ir Instrument

by groupe lépine

Identity

Trade Name
ARAMIS STEM IMPACTOR EUDAMED
Device Name
Class Ir Instrument EUDAMED
Model / Reference
Class Ir Instrument EUDAMED
ETA IMPT EUDAMED

Identifiers

Primary DI / UDI-DI
+M483ETAIMPT0 EUDAMED
Basic UDI-DI
++M483L0911YN EUDAMED
Direct Marketing DI
+M483ETAIMPT0 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 Stem Impactor 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 35b029db-021d-4bca-a3ee-a2af3bd87203 61 fields · synced Jul 10, 2026