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ARAMIS Graft Reamer Ø28

EUDAMED

Class I (EU MDR)

Ref EAA SC28Model EAA SC25

by groupe lépine

Identity

Trade Name
ARAMIS Graft Reamer Ø28 EUDAMED
Device Name
ARAMIS Graft Reamer Ø25 EUDAMED
Model / Reference
EAA SC25 EUDAMED
EAA SC28 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483EAASC280 EUDAMED
Basic UDI-DI
++M483L091102F5 EUDAMED
Direct Marketing DI
+M483EAASC280 EUDAMED
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE 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

Category: Acetabular orthopaedic reamer

ARAMIS Graft Reamer Ø28 by groupe lépine — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

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 7522d76c-5cb7-4812-b49f-831558bf2073 61 fields · synced Jul 31, 2026