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Flex 24

by Teknimed SAS

Part of a family of 14 devices: see the family page

Ref T040324Model Radiopaque bone cement

Flex 24 (T040324) is a Class III device made by Teknimed, registered in EUDAMED on 30 Jul 2024 (Basic UDI-DI 376017704B04CY), active as of 7 Nov 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376017704B04CY Basic UDI-DI 03760177047051UDI-DIDate30 Jul 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Highv+
Model / reference
Radiopaque bone cement, T040324
Primary DI / UDI-DI
03760177047051
Basic UDI-DI
376017704B04CY
EMDN code
P900403 Non-resorbable filling and reconstruction devices
Device class
Class III
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001224

Similar devices in this category

Other devices filed under NON-RESORBABLE FILLING AND RECONSTRUCTION DEVICES.

Other devices from Teknimed

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Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)