Skip to content

Plate pusher

by adapsia

Ref 230-299, 230-300

Plate pusher (230-299) is a Class I device made by adapsia, registered in EUDAMED on 8 Apr 2026 (Basic UDI-DI 36639173320SK), 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 Number36639173320SK Basic UDI-DI Date8 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade name
Plate pusher
Plate pusher for high osteotomy
Device name
Positioning instrument curved
Model / reference
230-299, 230-300
Primary DI / UDI-DI
03663917008605, 03663917007271
Basic UDI-DI
36639173320SK
EMDN code
L091002 Instruments for processing materials for osteosynthesis, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000011356

Similar devices in this category

Other devices filed under INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from adapsia

See all devices from adapsia →

Properties

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