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Cannulated Reamer

by LIMACORPORATE S.p.A.

Part of a family of 53 devices: see the family page

Ref 9CC0.30.032Model 80333902A002BC, Cannulated Reamer

Cannulated Reamer (9CC0.30.032) is a Class IIa device made by LIMACORPORATE S.p.A., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 80333902A002BC), active as of 7 Nov 2026.

Active European Union

CE MDR CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number80333902A002BC Basic UDI-DI 08033390131025UDI-DIDate29 Oct 2026RegisteredStatusActive
European UnionCE/MDR Number80333902A002BC Basic UDI-DI 08033390131025UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Model / reference
80333902A002BC, 9CC0.30.032, Cannulated Reamer
Primary DI / UDI-DI
08033390131025
Basic UDI-DI
80333902A002BC, B-08033390131025
EMDN code
L091102 Orthopaedic prostheses reamers and burs, reusable
Device class
Class IIa
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000010690

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE.

Other devices from LIMACORPORATE S.p.A.

See all devices from LIMACORPORATE S.p.A. →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)