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Guide Wire
EUDAMEDClass IIa (EU MDR)
Ref FG2300Model FG2300, FG2301, FG2302, KMC-000-00, KMC-000-10
Identity
- Device Name
- Guide Wire EUDAMED
- Model / Reference
- FG2300, FG2301, FG2302, KMC-000-00, KMC-000-10 EUDAMEDFG2300 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06938695523037 EUDAMED
- Basic UDI-DI
- 69386955KT0423 EUDAMED
- Direct Marketing DI
- 06938695523037 EUDAMED
- EMDN Code
- P099002 ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Guide Wire by Shanghai Kinetic Medical Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 69386955KT0423 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Shanghai Kinetic Medical Co., Ltd.
- EUDAMED SRN
- CN-MF-000017688
- Authorised Representative
- Prolinx GmbH DE-AR-000005129
Sources (1)
- EUDAMED 64f142fe-8975-46c9-8fdc-5d90d7b50112 61 fields · synced Oct 6, 2026