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Didposable Virus Sampling Tube

by Nanjing Norman Biological Technology Co., Ltd. 14 variants

Ref 22202700100115Model 240μL/tube,300μL/tube,400μL/tube,500μL/tube,600μL/tube,800μL/tube,1mL/tube,1.5mL/tube,2.0mL/tube,2.5mL/tube,3.0mL/tube,3.5mL/tube,5mL/tube,6mL/tube

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 Number69218930060086J Basic UDI-DI 06921893006389UDI-DIDate11 Aug 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Didposable Virus Sampling Tube
Model / Reference
240μL/tube, 300μL/tube, 400μL/tube, 500μL/tube, 600μL/tube, 800μL/tube, 1mL/tube, 1.5mL/tube, 2.0mL/tube, 2.5mL/tube, 3.0mL/tube, 3.5mL/tube, 5mL/tube, 6mL/tube, 22202700100115
Primary DI / UDI-DI
06921893006389
Basic UDI-DI
69218930060086J
EMDN Code
W05019099 Samples collection devices - other
Device Class
Class A
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000024233
Authorised representative
Sungo Cert GmbH DE-AR-000010869

Other devices from Nanjing Norman Biological Technology Co., Ltd.

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Properties

  • Professional Testing

Other properties (10)

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