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Anc062029

EUDAMED

Class IIa (EU MDR)

Ref ANC062029Model Trial Implants -Hip

by X.nov Medical Technology

Identity

Model / Reference
Trial Implants -Hip EUDAMED
ANC062029 EUDAMED

Identifiers

Primary DI / UDI-DI
03700535170120 EUDAMED
Basic UDI-DI
3700535100015PS EUDAMED
Direct Marketing DI
03700535170120 EUDAMED
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER 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

Anc062029 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 bdebf98c-2195-4eb1-a3d8-2cf42998101b 61 fields · synced Jul 31, 2026