Skip to content

FlexiRest Left M

by Catell AB

Part of a family of 353 devices: see the family page

Ref 7760-23

FlexiRest Left M (7760-23) is a Class I device made by Catell AB, registered in EUDAMED on 27 May 2025 (Basic UDI-DI 734020216M6), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number734020216M6 Basic UDI-DI 07340202109938UDI-DIDate27 May 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  • Withdrawn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
Hand
Model / reference
7760-23
Primary DI / UDI-DI
07340202109938
Basic UDI-DI
734020216M6
EMDN code
Y060606 Hand orthoses
Device class
Class I
EU registration type
Standard device
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000000726

Similar devices in this category

Other devices filed under UPPER EXTREMITY ORTHOSES (SPLINTS AND BRACES).

Other devices from Catell AB

See all devices from Catell AB →

Properties

Other properties (14, all answered No)