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Liposorber

by KANEKA Corporation

Ref LA-15Model LIPOSORBER LA-15, LIPOSORBER

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4993478KNK00642 Basic UDI-DI 04993478010021UDI-DIDate20 Oct 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  • Withdrawn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

Trade Name
Liposorber
Liposorber (La-15)
Device Name
La-15
Model / Reference
LIPOSORBER LA-15, LA-15, LIPOSORBER
Primary DI / UDI-DI
04993478010021
Basic UDI-DI
4993478KNK00642, B-04993478010021
EMDN Code
B030201 Plasmapheresis devices and kits
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000022143
Authorised representative
Kaneka Medical Europe N.V. BE-AR-000010091

Other devices from Kaneka Corp.

See all devices from Kaneka Corp. →

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