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Phlebo Press

by Mego Afek AC Ltd. EUDAMED

Active European Union

Ref L10006D2-EU, L10006D7-EUModel 603, 650

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number729010587603CK Basic UDI-DIDate27 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Phlebo Press DVT
Phlebo Press DVT 650 Easy
Model / Reference
603, L10006D2-EU, 650, L10006D7-EU
Primary DI / UDI-DI
07290105871411, 07290105879448
Basic UDI-DI
729010587603CK, 729010587650CU
Direct Marketing DI
07290105871411
07290105879448
EMDN Code
Z120607 Pneumatic compression equipment
Device Class
Class IIa
Market of Registration
Spain
France

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

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