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Osteotome, 20mm

by Intrauma S.p.A.

Part of a family of 33 devices: see the family page

Ref S9904Model str.001

Osteotome, 20mm (S9904) is a Class I device made by Intrauma S.p.A., registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 8056693101AF), active as of 7 Nov 2026.

Active European Union

CE MDR

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 Number8056693101AF Basic UDI-DI 08056693087875UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Instruments for drilling
Model / reference
str.001, S9904
Primary DI / UDI-DI
08056693087875
Basic UDI-DI
8056693101AF
Direct marketing DI
08056693087875
EMDN code
L090401 Orthopaedic surgery osteotomes, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000005991

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY OSTEOTOMES, REUSABLE.

Other devices from Intrauma S.p.A.

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

Properties

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