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Activmotion S DTO

by Newclip Technics SAS 15 variants

Ref ZCTDMD1-ST

Activmotion S DTO (ZCTDMD1-ST) is a Class IIb device made by Newclip Technics SAS, registered in EUDAMED on 3 Nov 2025 (Basic UDI-DI 3700569600158V), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3700569600158V Basic UDI-DI 03700569676490UDI-DIDate3 Nov 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Activmotion S DTO
Model / reference
ZCTDMD1-ST
Primary DI / UDI-DI
03700569676490
Basic UDI-DI
3700569600158V
EMDN code
P09120599 Bone fixation plates - other
Device class
Class IIb
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000011809

Other devices from Newclip Technics SAS

See all devices from Newclip Technics SAS →

Properties

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