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TAONET Pro

by Roche Diagnostics, S.L.U.

Ref 09230823001Model TAONET Pro Mobile interface

Active European Union

CE IVDR

Valid until

31 Aug 2028

CE IVDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV Rheinland LGA Products GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8430215TAONETUF Basic UDI-DI 08430215058268UDI-DIDate9 Sep 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • IX 1767578-1 Active Supplemented

    Technical documentation EU IVDR

    Certifier
    TÜV Rheinland LGA Products GmbH 0197
    Issued
    7 Apr 2025
    Expires
    31 Aug 2028
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / Reference
TAONET Pro Mobile interface, 09230823001
Primary DI / UDI-DI
08430215058268
Basic UDI-DI
8430215TAONETUF
Direct Marketing DI
08430215058268
EMDN Code
W0201010192 Chemistry analysers - IVD medical device software
Device Class
Class C
Special Device Type
Software
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000000700

Other devices from Roche Diagnostics, S.L.U.

Properties

  • Self Testing
  • Near-Patient Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No