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Patellar Reamer Guide Dia 35

by LIMACORPORATE S.p.A.

Ref 9CC0.65.019Model 80333902A040BL, Patellar Reamer Guide Dia 35

Active European Union

CE MDR CE MDD

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number80333902A040BL Basic UDI-DI 08033390125888UDI-DIDate29 Oct 2026RegisteredStatusActive
European UnionCE/MDR Number80333902A040BL Basic UDI-DI 08033390125888UDI-DIDate29 Oct 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  • Withdrawn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/MDD, CE/MDR Active

Specification

EUDAMED

Model / Reference
80333902A040BL, 9CC0.65.019, Patellar Reamer Guide Dia 35
Primary DI / UDI-DI
08033390125888
Basic UDI-DI
80333902A040BL, B-08033390125888
EMDN Code
L0922, L091199
Device Class
Class IIa
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000010690

Other devices from LIMACORPORATE S.p.A.

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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