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9735030

by Medtronic Navigation Inc.

Ref 9735030

9735030 is a device classified as Class I in the EU and Class II in the US made by Medtronic Navigation Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 0763000B00009488P) and listed in FDA GUDID since 10 Nov 2019 (UDI-DI 00763000210359), active as of 8 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0763000B00009488P Basic UDI-DI 00763000210359UDI-DIDate28 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00763000210359 UDI-DI Date10 Nov 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0763000B00009488P registered 28 Oct 2026 Active
  • FDA GUDID UDI-DI 00763000210359 listed 10 Nov 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00763000210359
  2. Registered EUDAMED 0763000B00009488P

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Neurological stereotactic surgery system
Model / reference
9735030
Primary DI / UDI-DI
00763000210359
Basic UDI-DI
0763000B00009488P
FDA product code
HAW
EMDN code
Z12011480 Surgical navigation instruments - hardware accessories
GMDN term
Neurological stereotactic surgery system
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.4560
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
Този процедурен пакет е предназначен за навигирана черепна хирургия
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Neurological stereotactic surgery system

Similar devices in this category

Other devices filed under SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Medtronic Navigation Inc.

See all devices from Medtronic Navigation Inc. →

Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
Other properties (12, all answered No)