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Rod Holder II

by Tianjin Zhengtian Medical Instrument Co., Ltd.

Ref A44022, A42019

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-CNMF0000201151814J7 Basic UDI-DI Date15 Sep 2024RegisteredStatusActive

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  • Withdrawn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
Rod Holder II
Rod Holder
Model / Reference
A44022, A42019
Primary DI / UDI-DI
D-CNMF0000201151814J7, D-CNMF0000201151804J4
Basic UDI-DI
B-CNMF0000201151814J7, B-CNMF0000201151804J4
EMDN Code
L091104, L091101
Device Class
Class I
Market of Registration
Spain

Manufacturer details

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

Related devices

Category: Orthopaedic implant impactor, reusable

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