Skip to content

spinit®

by biosurfit SA Portugal EUDAMED

Ref 240300Model spinit® CRP

EMDN W01021109

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-240300MC Basic UDI-DIDate8 Mar 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/IVDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
spinit® CRP
Model / Reference
spinit® CRP, 240300
Primary DI / UDI-DI
D-240300MC
Basic UDI-DI
B-240300MC
EMDN Code
W01021109 C-reactive protein
Device Class
Class IVD General
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000033920

Other devices from biosurfit SA

See all devices from biosurfit SA →

Properties & raw data

Show properties, registry sources and raw records
  • Reagent
  • Near-Patient Testing
  • Professional Testing
Other properties (7)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED b9a507e4-0d32-4a86-bd45-d99a02e1a250 61 fields · synced 23 Oct 2026