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AG03-0832

by X.nov Medical Technology EUDAMED

Active European Union

Ref AG03-0832Model Knee instrumentation

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3700535100014PQ Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Model / Reference
Knee instrumentation, AG03-0832
Primary DI / UDI-DI
03700535132210
Basic UDI-DI
3700535100014PQ
Direct Marketing DI
03700535132210
EMDN Code
L0920 Orthopaedic surgery distractors, reusable
Device Class
Class I
Market of Registration
France

Manufacturer details

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

Other devices from X.nov Medical Technology

See all devices from X.nov Medical Technology →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No