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AFIAS Cyfra21-1

by Boditech Med Inc. EUDAMED

Active European Union

Ref SMFP-135Model AFIAS Cyfra21-1

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number880613300640CD Basic UDI-DIDate28 Jun 2026RegisteredStatusActive
European UnionCE/IVDR Number880613300640CD Basic UDI-DIDate28 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDD, CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
AFIAS Cyfra21-1, SMFP-135
Primary DI / UDI-DI
08806133043967, 08806133006405
Basic UDI-DI
880613300640CD, B-08806133006405
EMDN Code
W0102030111 Cyfra 21-1
Device Class
Class C
Class IVD General
Market of Registration
Austria
Italy

Manufacturer details

EUDAMED SRN
KR-MF-000011028
Authorised representative
Obelis s.a. BE-AR-000000106

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Properties

Show properties
  • Animal Tissues
  • Microbial Substances NoEUDAMEDYesEUDAMED
  • Reagent
  • Professional Testing
Other properties (7)
  • Sterile: No
  • Human Tissues: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No