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Pathogen Multiplex-PCR Library Prep Kit

by Shenzhen Health SwifTech Co., Ltd. 4 variants

Ref AA03-01-96D

Active European Union

CE IVDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697780576HSTAALIBGD7 Basic UDI-DI Date22 Mar 2025RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
AA03-01-96D
Primary DI / UDI-DI
06977805760160, 06977805760306
Basic UDI-DI
697780576HSTAALIBGD7
Direct Marketing DI
06977805760306
EMDN Code
W010699 Genetic tests - other
Device Class
Class A
EU market of registration
Türkiye
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000044339
Authorised representative
Medunion S.L. ES-AR-000019366

Other devices from Shenzhen Health SwifTech Co., Ltd.

Properties

  • Microbial Substances
  • Reagent
  • Professional Testing
  • New Device NoEUDAMEDYesEUDAMED

Other properties (7)

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