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LimFlow V-Ceiver

by LimFlow SA EUDAMED

Active European Union

Ref VC-CE-21

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000261596 Date21 Aug 2025IssuedStatusActive expires 26 Oct 2028

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000261596 Issued

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    21 Aug 2025
    Expires
    26 Oct 2028

Specification

EUDAMED

Model / Reference
VC-CE-21
Primary DI / UDI-DI
00850017630291
Basic UDI-DI
0850017630VCCE21RS
EMDN Code
C010102 Peripheral i.v. catheter systems
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000011529

Other devices from LimFlow SA

See all devices from LimFlow SA →

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