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Apparato per pressoterapia sequenziale mod. AFP 250 DIGITAL

by FISIOPRESS srl EUDAMED

Active European Union

Ref AFP 250 DIGITALModel APPARATO PER PRESSOTERAPIA SEQUENZIALE

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805414119000AFP4CE Basic UDI-DIDate10 Sep 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  • Withdrawn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
Apparato per Pressoterapia Sequenziale
Model / Reference
APPARATO PER PRESSOTERAPIA SEQUENZIALE, AFP 250 DIGITAL
Primary DI / UDI-DI
08054141190993
Basic UDI-DI
805414119000AFP4CE
Direct Marketing DI
08054141190993
EMDN Code
Z120607 Pneumatic compression equipment
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000026366

Other devices from FISIOPRESS srl

See all devices from FISIOPRESS srl →

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