Skip to content

INNOVIQURE AMH Reagent Kit

by Deni̇z Bi̇yoki̇mya Ürünleri̇ Diş Ti̇c. A.Ş. Gazi̇emi̇r İzmi̇r Şubesi̇

Ref 733277Model 200T

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-8683981733277GF Basic UDI-DI D-8683981733277GFUDI-DIDate5 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Model / Reference
200T, 733277
Primary DI / UDI-DI
D-8683981733277GF
Basic UDI-DI
B-8683981733277GF
EMDN Code
W0102050215 Anti-mullerian hormone
Device Class
Class IVD General
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000034179

Other devices from Deni̇z Bi̇yoki̇mya Ürünleri̇ Diş Ti̇c. A.Ş. Gazi̇emi̇r İzmi̇r Şubesi̇

See all devices from Deni̇z Bi̇yoki̇mya Ürünleri̇ Diş Ti̇c. A.Ş. Gazi̇emi̇r İzmi̇r Şubesi̇ →

Properties

  • Reagent
  • Professional Testing

Other properties (8)

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