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FT3 Test Cassette

by Hangzhou Alltest Biotech.Co., Ltd. 2 variants

Ref FI-FT3-402

FT3 Test Cassette (FI-FT3-402) is a device classified as IVD General made by Hangzhou Alltest Biotech.Co., Ltd., registered in EUDAMED on 26 Aug 2026 (Basic UDI-DI B-FI-FT3-402KQ), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-FI-FT3-402KQ Basic UDI-DI Date26 Aug 2026RegisteredStatusActive

Official records

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  • Withdrawn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
FI-FT3-402
Primary DI / UDI-DI
D-FI-FT3-402KQ, 06942598251003
Basic UDI-DI
B-FI-FT3-402KQ, B-06942598251003
EMDN code
W01020401 Free triiodothyronine
Device class
Class IVD General
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000010710
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under FREE TRIIODOTHYRONINE.

Other devices from Hangzhou Alltest Biotech.Co., Ltd.

See all devices from Hangzhou Alltest Biotech.Co., Ltd. →

Properties

  • Contains animal tissues or cells NoEUDAMEDYesEUDAMED
  • Reagent NoEUDAMEDYesEUDAMED
  • IVD kit
  • Professional testing
Other properties (9, all answered No)