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Cascadeflo EC

by Sb-Kawasumi Laboratories, Inc. 4 variants

Ref EC-30W

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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 Number4987488PCS_EC_PW Basic UDI-DI 04987488102142UDI-DIDate8 Jul 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Plasma Component Separator
Model / Reference
EC-30W
Primary DI / UDI-DI
04987488102142
Basic UDI-DI
4987488PCS_EC_PW
EMDN Code
B030201 Plasmapheresis devices and kits
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000011253
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Other devices from Sb-Kawasumi Laboratories, Inc.

See all devices from Sb-Kawasumi Laboratories, Inc. →

Properties

  • Sterile

Other properties (12)

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