Skip to content

Autoguide System

by Medtronic Navigation Inc.

Ref 29631

Autoguide System (29631) is a Class I device made by Medtronic Navigation Inc., registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI 0763000B00008388F), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0763000B00008388F Basic UDI-DI Date25 Sep 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Autoguide System
Model / reference
29631
Primary DI / UDI-DI
00763000705039, 00763000705053, 00763000704902, 00763000705091, 00763000480318, 00763000704919, 00763000704896, 00763000705060, 00763000705077, 00763000480288, 00763000704995
Basic UDI-DI
0763000B00008388F
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

Other properties (14, all answered No)