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XPER Technology PREMIUM

by TaiDoc Technology Corporation 6 variants

Ref TD-4370

XPER Technology PREMIUM (TD-4370) is a device classified as IVD Annex II List B made by Taidoc Technology Corporation, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-04719964610649), active as of 7 Nov 2026.

Active European Union

CE IVDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04719964610649 Basic UDI-DI 04719964610649UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Device name
Blood Glucose Test Strips
Model / reference
TD-4370
Primary DI / UDI-DI
04719964610649
Basic UDI-DI
B-04719964610649
EMDN code
W0101060101 Glucose test strips
Device class
Class IVD Annex II List B
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
TW-MF-000017956
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under GLUCOSE TEST STRIPS.

Other devices from Taidoc Technology Corporation

See all devices from Taidoc Technology Corporation →

Properties

  • Self-testing
  • Professional testing
  • Companion diagnostics
Other properties (9, all answered No)