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Smur Bras Rt

by Groupe Sober SAS

Ref SMUR BRAS RTModel ATTELLE DE SMUR RADIOTRANSPARENTE

Smur Bras Rt is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 20 Jul 2026 (Basic UDI-DI B-03701459800551), 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-03701459800551 Basic UDI-DI Date20 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  • Withdrawn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
ATTELLE DE SMUR RADIOTRANSPARENTE, SMUR BRAS RT
Primary DI / UDI-DI
03701459800551, 03701459800582, 03701459800575, 03701459800544, 03701459800568
Basic UDI-DI
B-03701459800551, B-03701459800582, B-03701459800575, B-03701459800544, B-03701459800568
EMDN code
Y060699 Orthoses, upper extremity - other
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 UPPER EXTREMITY ORTHOSES (SPLINTS AND BRACES).

Other devices from Groupe Sober SAS

See all devices from Groupe Sober SAS →

Properties

Other properties (12, all answered No)