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Eurospital - Test Di Gravidanza in Autodiagnosi

by Logiter One Srl

Ref TGLOG-14Model EUROSPITAL - TEST DI GRAVIDANZA

Active European Union

CE IVDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08050593875211 Basic UDI-DI 08050593875211UDI-DIDate12 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Model / Reference
EUROSPITAL - TEST DI GRAVIDANZA, TGLOG-14
Primary DI / UDI-DI
08050593875211
Basic UDI-DI
B-08050593875211
EMDN Code
W0102050205 Total human chorionic gonadotropin
Device Class
Class IVD devices for self-testing
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000037076

Other devices from Logiter One Srl

See all devices from Logiter One Srl →

Properties

  • Reagent
  • Self Testing

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No