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Lympha Press

by Mego Afek AC Ltd. Israel EUDAMED

Ref L10008C2-EUModel 912

EMDN Z120607

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number729010587912D3 Basic UDI-DIDate26 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Lympha Press Optimal Plus
Model / Reference
912, L10008C2-EU
Primary DI / UDI-DI
07290105879097
Basic UDI-DI
729010587912D3
Direct Marketing DI
07290105879097
EMDN Code
Z120607 Pneumatic compression equipment
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
IL-MF-000006982
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Mego Afek AC, Ltd.

See all devices from Mego Afek AC, Ltd. →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 173c2f7d-2f2f-4840-bd04-4bd7ebafcec4 61 fields · synced 22 Oct 2026