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Eezcare

by Eezcare Medical Corporation EUDAMED

Active European Union

Ref EzLymph_V1400002Model EzLymph M

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0471988335EEZ0600DX Basic UDI-DIDate19 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Lymphedema M Pump
Model / Reference
EzLymph M, EzLymph_V1400002
Primary DI / UDI-DI
04719883355003
Basic UDI-DI
0471988335EEZ0600DX
EMDN Code
Z12069099 Various physiotherapy and rehabilitation instruments - other
Device Class
Class IIa
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
TW-MF-000018338
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Eezcare Medical Corp

See all devices from Eezcare Medical Corp →

Properties

Other properties (13)

  • Sterile: No
  • 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