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Rotax Trial Anchor. Stem L105

EUDAMED

Class IIa (EU MDR)

Ref K193105Model Orthopaedic prostheses positioners, reusable

by groupe lépine

Identity

Trade Name
ROTAX TRIAL ANCHOR. STEM L105 EUDAMED
Device Name
Orthopaedic prostheses positioners, reusable EUDAMED
Model / Reference
Orthopaedic prostheses positioners, reusable EUDAMED
K193105 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483K1931050 EUDAMED
Basic UDI-DI
++M483L091104F9 EUDAMED
Direct Marketing DI
+M483K1931050 EUDAMED
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED

Classification

Device Class
Class IIa 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

Rotax Trial Anchor. Stem L105 by groupe lépine — Class IIa — 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 bb1edcb4-e658-4e6c-863e-8ab0db9b1234 61 fields · synced Jun 19, 2026