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Pecopen 080

by Infomed SA Switzerland EUDAMED

Ref DF-080-00Model Hemofilter

EMDN F010604

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07640137441036 Basic UDI-DIDate5 Feb 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
Hemofilter, DF-080-00
Primary DI / UDI-DI
07640137441036
Basic UDI-DI
B-07640137441036
EMDN Code
F010604 Dialysers for special haemodiafiltration and other therapies
Device Class
Class IIb
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CH-MF-000021686
Authorised representative
INFOMED SAS FR-AR-000009093

Other devices from Infomed SA

See all devices from Infomed SA →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 2c9601d7-4411-4248-9496-de94ab1bb23c 61 fields · synced 22 Oct 2026