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COVID-19 (SARS-CoV-2) Antigen TestKit(Colloidal Gold)

by Anhui Deepblue Medical Technology Co., Ltd

Ref SL030101NST-2Model Cassette

Active European Union

CE IVDR

Valid until

21 Mar 2030

CE IVDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Kiwa Sertio Oy

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberEU-TDA-FI-20642-800030-2025-1 Date9 Jun 2026IssuedStatusActive expires 21 Mar 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EU-TDA-FI-20642-800030-2025-1 Active Supplemented

    Technical documentation EU IVDR

    Certifier
    Kiwa Sertio Oy 3018
    Issued
    9 Jun 2026
    Expires
    21 Mar 2030
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)
Model / Reference
Cassette, SL030101NST-2
Primary DI / UDI-DI
06952062712954
Basic UDI-DI
69520627J012L3
Unit of Use DI
06952062712718
EMDN Code
W0105099099 Virology - rt & poc - other
Device Class
Class C
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000018785
Authorised representative
Mega Eurostar Sp. z o.o. PL-AR-000042730

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Properties

  • Self Testing

Other properties (10)

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