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Universal Drill Guides

by Medtronic Navigation Inc.

Ref 9733457

Universal Drill Guides (9733457) is a Class I device made by Medtronic Navigation Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 0763000B00000917B), active as of 8 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0763000B00000917B Basic UDI-DI 00763000342258UDI-DIDate28 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Universal Drill Guides
Model / reference
9733457
Primary DI / UDI-DI
00763000342258
Basic UDI-DI
0763000B00000917B
EMDN code
Z12011480 Surgical navigation instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000023263
Authorised representative
Medtronic B.V. NL-AR-000006050

Other devices from Medtronic Navigation Inc.

See all devices from Medtronic Navigation Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
Other properties (11, all answered No)