Skip to content

Pre-Reamer Drill

by LIMACORPORATE S.p.A.

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

Ref 9051.10.015Model Pre-Reamer Drill, 80333902A005BJ

Pre-Reamer Drill (9051.10.015) is a Class IIa device made by LIMACORPORATE S.p.A., registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-08033390117258), 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/MDR NumberB-08033390117258 Basic UDI-DI 08033390117258UDI-DIDate6 Nov 2026RegisteredStatusActive
European UnionCE/MDD NumberB-08033390117258 Basic UDI-DI 08033390117258UDI-DIDate6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Specification

EUDAMED

Model / reference
Pre-Reamer Drill, 9051.10.015, 80333902A005BJ
Primary DI / UDI-DI
08033390117258
Basic UDI-DI
B-08033390117258, 80333902A005BJ
EMDN code
L091102, L091199
Device class
Class IIa
EU registration type
Legacy device (under a directive)
Standard device
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)