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Aramis T-Handle

EUDAMED

Class I (EU MDR)

Ref EAA PT00Model Class I Instrument

by groupe lépine

Identity

Trade Name
ARAMIS T-HANDLE EUDAMED
Device Name
Class I Instrument EUDAMED
Model / Reference
Class I Instrument EUDAMED
EAA PT00 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483EAAPT000 EUDAMED
Basic UDI-DI
++M483L0999ZW EUDAMED
Direct Marketing DI
+M483EAAPT000 EUDAMED
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY 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 T-Handle 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 20ebcd26-1773-4077-9afe-2a57c53525b8 61 fields · synced Jun 19, 2026