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Plate Bender

by Tianjin Zhengtian Medical Instrument Co., Ltd. 8 variants

Ref A63031

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-CNMF0000201151977K4 Basic UDI-DIDate17 Mar 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Plate Bender
Model / Reference
A63031
Primary DI / UDI-DI
D-CNMF0000201151977K4
Basic UDI-DI
B-CNMF0000201151977K4
EMDN Code
L091101 Orthopaedic prostheses and traumatological implants extractors, reusable
Device Class
Class I
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000020115
Authorised representative
Inion Oy FI-AR-000046224

Other devices from Tianjin Zhengtian Medical Instrument Co., Ltd.

See all devices from Tianjin Zhengtian Medical Instrument Co., Ltd. →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No