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Ah50-2208

EUDAMED

Class I (EU MDR)

Ref AH50-2208Model Hip instrumentation

by X.nov Medical Technology

Identity

Model / Reference
Hip instrumentation EUDAMED
AH50-2208 EUDAMED

Identifiers

Primary DI / UDI-DI
03700535161227 EUDAMED
Basic UDI-DI
3700535100012PL EUDAMED
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE 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

For the AH50-2208 medical device, this comprehensive directory provides detailed information on its X.NOV medical technology, including its purpose, classification, and specifications. By understanding the device's key features and compliance status, healthcare professionals can make informed decisions about its use and implementation.

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 585bf523-38db-49e7-bcb5-f2b7765c20d0 61 fields · synced Oct 6, 2026