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Community Modular Foam

by Harvest Healthcare United Kingdom EUDAMED

Ref HFC129.01BR Model Community Modular Foam 

EMDN V08030101

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506051753HHUK00282 Basic UDI-DIDate12 May 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
Community Modular Foam
Model / Reference
Community Modular Foam, HFC129.01BR
Primary DI / UDI-DI
05060517531560
Basic UDI-DI
506051753HHUK00282
EMDN Code
V08030101 Active anti-decubitus medical cushions
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000011160
Authorised representative
Evolution Healthcare Ltd XI-AR-000047925

Other devices from Harvest Healthcare

See all devices from Harvest Healthcare →

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 37f4e123-03d9-4d29-b9df-fb709b7041aa 61 fields · synced 22 Oct 2026