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INTERCEPT Processing Set for Plasma

by Cerus Corporation 2 variants

Ref INT3104B, INT3104Model INT31

Active European Union

CE MDR

Valid until

23 Aug 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

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/MDR Number872058919008PLS2R Basic UDI-DI 18717953197112UDI-DIDate7 Mar 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
INT31, INT3104B, INT3104
Primary DI / UDI-DI
18717953197112
Basic UDI-DI
872058919008PLS2R
EMDN Code
B010199 Blood collection bags and kits - other
Device Class
Class III
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
US-MF-000000765
Authorised representative
Cerus Europe B.V. NL-AR-000000115

Other devices from Cerus Corporation

See all devices from Cerus Corporation →

Properties

  • Sterile
  • Endocrine Disruptor

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No