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Contre Couple

by Clariance 2 variants

Part of a family of 10 devices: see the family page

Ref 50721000Model Spinal instrumentation

Contre Couple (50721000) is a Class I device made by Clariance-SAS, registered in EUDAMED on 7 Jul 2026 (Basic UDI-DI 0370078069903CCE3), active as of 22 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0370078069903CCE3 Basic UDI-DI 03700780629695UDI-DIDate7 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Spinal instrumentation, 50721000
Primary DI / UDI-DI
03700780629695
Basic UDI-DI
0370078069903CCE3
EMDN code
P090799 Spinal prostheses and stabilisation systems - other
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000023666

Similar devices in this category

Other devices filed under SPINAL PROSTHESES AND STABILISATION SYSTEMS - OTHER.

Other devices from Clariance-SAS

See all devices from Clariance-SAS →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)