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Tactile Probe

by Medtronic Navigation Inc.

Ref 9734435

Tactile Probe (9734435) is a Class I device made by Medtronic Navigation Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 0763000B000008178), 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 Number0763000B000008178 Basic UDI-DI 00763000339203UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Tactile Probe
Model / reference
9734435
Primary DI / UDI-DI
00763000339203
Basic UDI-DI
0763000B000008178
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)