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Plates Activmotion S

by Newclip Technics SAS 14 variants

Part of a family of 52 devices: see the family page

Ref AETGP1D

Plates Activmotion S (AETGP1D) is a Class IIb device made by Newclip Technics SAS, registered in EUDAMED on 9 Sep 2025 (Basic UDI-DI 3700569600248W), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3700569600248W Basic UDI-DI 03700569629670UDI-DIDate9 Sep 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Plates Activmotion S
Model / reference
AETGP1D
Primary DI / UDI-DI
03700569629670
Basic UDI-DI
3700569600248W
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

Similar devices in this category

Other devices filed under BONE FIXATION PLATES - OTHER.

Other devices from Newclip Technics SAS

See all devices from Newclip Technics SAS →

Properties

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