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Coudocor Light

by Groupe Sober SAS

Ref COUDOCOR LIGHTModel ECHARPE COUDE AU CORPS LEGERE

Coudocor Light is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 21 Jul 2026 (Basic UDI-DI B-03701459802746), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03701459802746 Basic UDI-DI Date21 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  • Withdrawn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

Model / reference
ECHARPE COUDE AU CORPS LEGERE, COUDOCOR LIGHT
Primary DI / UDI-DI
03701459802746, 03701459802753, 03701459802777, 03701459802760, 03701459802784
Basic UDI-DI
B-03701459802746, B-03701459802753, B-03701459802777, B-03701459802760, B-03701459802784
EMDN code
M030501 Immobilisation bandages for shoulder, arm and collarbone
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 IMMOBILISATION BANDAGES FOR SHOULDER, ARM AND COLLARBONE.

Other devices from Groupe Sober SAS

See all devices from Groupe Sober SAS →

Properties

Other properties (12, all answered No)