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Pressoterapia FP4 Venosanpress

by FISIOPRESS srl EUDAMED

Active European Union

Ref FP4 VENOSANPRESS

Overview

Discover the PRESSOTERAPIA FP4 VENOSANPRESS, a high-quality medical device designed for sequential endoscopy, offering improved diagnostic accuracy and patient comfort. Learn about its features, compliance, and regulatory status.

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08054141190047 Basic UDI-DIDate6 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD 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
Dispositivo per la PRESSOTERAPIA SEQUENZIALE
Model / Reference
FP4 VENOSANPRESS
Primary DI / UDI-DI
08054141190047
Basic UDI-DI
B-08054141190047
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 (11)

  • Sterile: No
  • 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