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Smur Jambe Rt

by Groupe Sober SAS

Ref SMUR JAMBE RTModel ATTELLE SMUR RADIOTRANSPARENTE, ATTELLE SMUR RT

Smur Jambe Rt is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 22 Jul 2026 (Basic UDI-DI B-03701459806386), 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-03701459806386 Basic UDI-DI Date22 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  • Withdrawn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 SMUR RADIOTRANSPARENTE, SMUR JAMBE RT, ATTELLE SMUR RT
Primary DI / UDI-DI
03701459806386, 03701459806393, 03701459806409, 03701459806362, 03701459806416, 03701459806379, 03701459806355
Basic UDI-DI
B-03701459806386, B-03701459806393, B-03701459806409, B-03701459806362, B-03701459806416, B-03701459806379, B-03701459806355
EMDN code
Y06121201 Passive knee-ankle-foot 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

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Properties

Other properties (12, all answered No)