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Inst Kit 9735028 Cranial EU Only

by Medtronic Navigation Inc.

Ref 9735028

Inst Kit 9735028 Cranial EU Only is a Class III device made by Medtronic Navigation Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 0763000B00008147Z), 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 Number0763000B00008147Z Basic UDI-DI Date28 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Inst Kit 9735028 Cranial EU Only
Model / reference
9735028
Primary DI / UDI-DI
00763000922436, 00763000154172, 00763000922429, 00763000701413
Basic UDI-DI
0763000B00008147Z
EMDN code
Z12011480 Surgical navigation instruments - hardware accessories
Device class
Class III
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
Този процедурен пакет е предназначен за навигирана черепна хирургия

Manufacturer details

EUDAMED SRN
US-PR-000014543

Other devices from Medtronic Navigation Inc.

See all devices from Medtronic Navigation Inc. →

Properties

Other properties (2, all answered No)