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Anc02613

EUDAMED

Class IIa (EU MDR)

Ref ANC02613Model Trial Implants -Hip

by X.nov Medical Technology

Identity

Model / Reference
Trial Implants -Hip EUDAMED
ANC02613 EUDAMED

Identifiers

Primary DI / UDI-DI
03700535173664 EUDAMED
Basic UDI-DI
3700535100015PS EUDAMED
Direct Marketing DI
03700535173664 EUDAMED
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, 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

Anc02613 by X.nov Medical Technology — 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

EUDAMED SRN
CH-MF-000018319
Authorised Representative
X.NOV FR-AR-000007682

Sources (1)

  • EUDAMED 37b12801-1fd8-4726-8c6f-ef303c1785d4 61 fields · synced Jul 31, 2026