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Wire Guide

EUDAMED

Class I (EU MDR)

Ref C65010Ref C53005Ref C65005

by Tianjin Zhengtian Medical Instrument Co., Ltd.

Identity

Device Name
Wire Guide EUDAMED
Model / Reference
C65010 EUDAMED
C53005 EUDAMED
C65005 EUDAMED

Identifiers

Primary DI / UDI-DI
D-CNMF0000201150507HL EUDAMED
D-CNMF0000201150418HL EUDAMED
D-CNMF0000201150501H8 EUDAMED
Basic UDI-DI
B-CNMF0000201150507HL EUDAMED
B-CNMF0000201150418HL EUDAMED
B-CNMF0000201150501H8 EUDAMED
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Orthopaedic implant impactor, reusable

Wire Guide by Tianjin Zhengtian Medical Instrument Co., Ltd. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

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

Sources (3)

  • EUDAMED db3c72d5-288a-4ddc-8c92-ebbd0fa20357 61 fields · synced Aug 1, 2026
  • EUDAMED 51703a96-61b0-45d1-8593-ac1b3688bb1f 61 fields · synced May 17, 2026
  • EUDAMED 90873d9d-2578-45fe-bed5-db8ab4b53406 61 fields · synced May 18, 2026