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Podosil

by Thuasne Deutschland GmbH 5 variants

Ref T47880104001499, T47880103601499, T47880104201499

Podosil (T47880104001499) is a Class I device made by Thuasne Deutschland GmbH, registered in EUDAMED on 8 Dec 2025 (Basic UDI-DI 4035459DE1102A2V), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4035459DE1102A2V Basic UDI-DI Date8 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  • Withdrawn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
Podosil
Model / reference
T47880104001499, T47880103601499, T47880104201499
Primary DI / UDI-DI
04035459084376, 04035459084352, 04035459084383
Basic UDI-DI
4035459DE1102A2V
Direct marketing DI
04035459084376
04035459084352
04035459084383
EMDN code
Y061203 Orthoses, foot (including insoles and inserts)
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
DE-MF-000006210

Similar devices in this category

Other devices filed under ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS).

Other devices from Thuasne Deutschland GmbH

See all devices from Thuasne Deutschland GmbH →

Properties

Other properties (14, all answered No)