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Physica ZUK - Femoral Preparation Instrument Set

by LIMACORPORATE S.p.A. 2 variants

Ref 9061.15.000Model Procedure pack for orthopedic surgery class IIa

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8033390KK200MY Basic UDI-DI 08033390325035UDI-DIDate12 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
8033390KK200MY
Model / Reference
Procedure pack for orthopedic surgery class IIa, 9061.15.000
Primary DI / UDI-DI
08033390325035
Basic UDI-DI
8033390KK200MY
EMDN Code
L0919 Orthopaedic and traumatological surgery instrument kits, reusable
Device Class
Class IIa
Medical Purpose
Orthopaedic and traumatological surgery instrument kits, reusable

Manufacturer details

EUDAMED SRN
IT-PR-000012691

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Properties

Other properties (1)

  • Sterile: No