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Carpatel - Tm/a

by Groupe Sober SAS

Ref CARPATELModel ATTELLE DE POIGNET

Carpatel - Tm/a is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 24 Jul 2026 (Basic UDI-DI B-03760035447085), active as of 24 Oct 2026.

Active European Union

CE MDD

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/MDD NumberB-03760035447085 Basic UDI-DI Date24 Jul 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Trade name
Carpatel - Tm/a
Carpatel - Tl/a
Carpatel - Ts/a
Device name
Carpatel
Model / reference
ATTELLE DE POIGNET, CARPATEL
Primary DI / UDI-DI
03760035447085, 03760035447092, 03760035447061
Basic UDI-DI
B-03760035447085, B-03760035447092, B-03760035447061
EMDN code
Y060609 Wrist (forearm) orthoses
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000017818

Similar devices in this category

Other devices filed under WRIST (FOREARM) ORTHOSES.

Other devices from Groupe Sober SAS

See all devices from Groupe Sober SAS →

Properties

Other properties (12, all answered No)