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Espaciadores de prueba rodilla Subiton

EUDAMED

Class IIa (EU MDR)

Ref 882010Model Rodilla

by Laboratorios SL S.A.

Identity

Trade Name
Espaciadores de prueba rodilla Subiton EUDAMED
Device Name
Espaciador de prueba de rodilla EUDAMED
Model / Reference
Rodilla EUDAMED
882010 EUDAMED

Identifiers

Primary DI / UDI-DI
07798034467328 EUDAMED
Basic UDI-DI
B-07798034467328 EUDAMED
EMDN Code
L098099 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER ACCESSORIES 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Espaciadores de prueba rodilla Subiton by Laboratorios SL S.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
AR-MF-000023153
Authorised Representative
Synergie Ingénierie Médicale FR-AR-000001802

Sources (1)

  • EUDAMED e8bc498b-9647-48ed-8c92-d21e9d4ec19f 61 fields · synced Aug 1, 2026