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Venoflex Micro

by Thuasne Deutschland GmbH 1,000+ variants

Ref 30023E21503021

Venoflex Micro (30023E21503021) is a Class I device made by Thuasne Deutschland GmbH, registered in EUDAMED on 19 Dec 2025 (Basic UDI-DI 4035459DE1406B3Y), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4035459DE1406B3Y Basic UDI-DI 04035459289269UDI-DIDate19 Dec 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Venoflex Micro
Model / reference
30023E21503021
Primary DI / UDI-DI
04035459289269
Basic UDI-DI
4035459DE1406B3Y
Direct marketing DI
04035459289269
EMDN code
M030405 Compression stockings
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
DE-MF-000006210

Related devices

Category: Compression/pressure sock/stocking, single-use

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Properties

Other properties (14, all answered No)