Skip to content

NADAL® Strep A Test

by nal von minden GmbH 3 variants

Ref 20122N20, 221001A, 222001A

Active European Union

CE IVDR CE IVDD

Valid until

2 Mar 2031

CE IVDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV Rheinland LGA Products GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number4065384STA1OPS4N1GXEW Basic UDI-DI Date23 Mar 2026RegisteredStatusActive
European UnionCE/IVDR Number4065384STA1OPS4N1GXEW Basic UDI-DI Date23 Mar 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD, CE/IVDR Active

Specification

EUDAMED

Device Name
Strep A Test
Model / Reference
20122N20, 221001A, 222001A
Primary DI / UDI-DI
04065384000172, D-nvm-221001AUW, D-nvm-222001AV9
Basic UDI-DI
4065384STA1OPS4N1GXEW, B-nvm-221001AUW, B-nvm-222001AV9
EMDN Code
W0105090103 Strep. a - rt & poc
Device Class
Class B
Class IVD General
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000013321

Other devices from nal von minden GmbH

See all devices from nal von minden GmbH →

Properties

  • Animal Tissues NoEUDAMEDYesEUDAMED
  • Microbial Substances YesEUDAMEDNoEUDAMED
  • Reagent NoEUDAMEDYesEUDAMED
  • Near-Patient Testing
  • Professional Testing

Other properties (6)

  • Sterile: No
  • Human Tissues: No
  • Self Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No