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INTERCEPT Processing Set for Platelets Dual Storage

by Cerus Corporation 3 variants

Ref INT25, INT2544B

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 18720589190020UDI-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  • Withdrawn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 1 Dec 2026
  • Belgium since 1 Dec 2026
  • Bulgaria since 1 Dec 2026
  • Croatia since 1 Dec 2026
  • Cyprus since 1 Dec 2026
  • Czechia since 1 Dec 2026
  • Denmark since 1 Dec 2026
  • Estonia since 1 Dec 2026
  • Finland since 1 Dec 2026
  • France since 1 Dec 2026
  • Germany since 1 Dec 2026
  • Greece since 1 Dec 2026
  • Hungary since 1 Dec 2026
  • Iceland since 1 Dec 2026
  • Ireland since 1 Dec 2026
  • Italy since 1 Dec 2026
  • Latvia since 1 Dec 2026
  • Liechtenstein since 1 Dec 2026
  • Lithuania since 1 Dec 2026
  • Luxembourg since 1 Dec 2026
  • Malta since 1 Dec 2026
  • Netherlands since 1 Dec 2026
  • Northern Ireland since 1 Dec 2026
  • Norway since 1 Dec 2026
  • Poland since 1 Dec 2026
  • Portugal since 1 Dec 2026
  • Romania since 1 Dec 2026
  • Slovakia since 1 Dec 2026
  • Slovenia since 1 Dec 2026
  • Spain since 1 Dec 2026
  • Sweden since 1 Dec 2026

Last checked 3 Nov 2026.

Specification

EUDAMED

Device Name
INTERCEPT Processing Set for Platelets
Model / Reference
INT25, INT2544B
Primary DI / UDI-DI
18720589190020
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
  • CMR Substance
  • Endocrine Disruptor

Other properties (10)

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