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INTERCEPT Processing Set for Platelets Large Volume

by Cerus Corporation 3 variants

Ref INT22, INT2203B

Active European Union

CE MDR

Valid until

2 Mar 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number872058919007PLT2L Basic UDI-DI 18717953197044UDI-DIDate6 Oct 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 104609 0007 Active Amended

    Technical documentation EU MDR

    Certifier
    TÜV SÜD Product Service GmbH 0123
    Issued
    31 Jul 2025
    Expires
    2 Mar 2028
    Reason
    Other

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 31 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 6 Jul 2006
  • Belgium since 6 Jul 2006
  • Bulgaria since 6 Jul 2006
  • Croatia since 6 Jul 2006
  • Cyprus since 6 Jul 2006
  • Czechia since 6 Jul 2006
  • Denmark since 6 Jul 2006
  • Estonia since 6 Jul 2006
  • Finland since 6 Jul 2006
  • France since 6 Jul 2006
  • Germany since 6 Jul 2006
  • Greece since 6 Jul 2006
  • Hungary since 6 Jul 2006
  • Iceland since 6 Jul 2006
  • Ireland since 6 Jul 2006
  • Italy since 6 Jul 2006
  • Latvia since 6 Jul 2006
  • Liechtenstein since 6 Jul 2006
  • Lithuania since 6 Jul 2006
  • Luxembourg since 6 Jul 2006
  • Malta since 6 Jul 2006
  • Netherlands since 6 Jul 2006
  • Northern Ireland since 6 Jul 2006
  • Norway since 6 Jul 2006
  • Poland since 6 Jul 2006
  • Portugal since 6 Jul 2006
  • Romania since 6 Jul 2006
  • Slovakia since 6 Jul 2006
  • Slovenia since 6 Jul 2006
  • Spain since 6 Jul 2006
  • Sweden since 6 Jul 2006

Last checked 3 Nov 2026.

Specification

EUDAMED

Device Name
INTERCEPT Processing Set for Platelets
Model / Reference
INT22, INT2203B
Primary DI / UDI-DI
18717953197044
Basic UDI-DI
872058919007PLT2L
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