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TMS Navigator Software

by Localite GmbH 6 variants

Part of a family of 12 devices: see the family page

Ref 010232Model TMS Navigator Software 3

TMS Navigator Software (010232), a medical device (EU MDR Class IIa; EMDN category medical device software - not included in other classes) made by LOCALITE GmbH, was registered in EUDAMED on 21 Apr 2023 (Basic UDI-DI ++G076A18R); registry data as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G076A18R Basic UDI-DI Date21 Apr 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
TMS Navigator Software
Model / reference
TMS Navigator Software 3, 010232
Primary DI / UDI-DI
+G076A010232AM3N30, +G076A010232AM3N40
Basic UDI-DI
++G076A18R
EMDN code
V92 Medical device software - not included in other classes
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005419

Similar devices in this category

Other devices filed under MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES.

Other devices from LOCALITE GmbH

See all devices from LOCALITE GmbH →

Properties

Other properties (14, all answered No)