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Trauma Instrument Set Series
EUDAMEDClass I (EU MDR)
Ref XC308Model XC101,XC102,XC103,XC104,XC105,XC106, XC107, XC108, XC109, XC110, XC111,XC112, XC113,XC114, XC115, XC116, XC201, XC301, XC302, XC303, XC304, XC305, XC306, XC307, XC308, XC309, XC310, XC311, XC312, XC313
Identity
- Device Name
- Trauma Instrument Set Series EUDAMED
- Model / Reference
- XC101,XC102,XC103,XC104,XC105,XC106, XC107, XC108, XC109, XC110, XC111,XC112, XC113,XC114, XC115, XC116, XC201, XC301, XC302, XC303, XC304, XC305, XC306, XC307, XC308, XC309, XC310, XC311, XC312, XC313 EUDAMEDXC308 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06975610802112 EUDAMED
- Basic UDI-DI
- 69756108002500YQ EUDAMED
- EMDN Code
- L0908 ORTHOPAEDIC AND TRAUMATOLOGICAL TRACTION INSTRUMENTS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Trauma Instrument Set Series by Changzhou Centrau Medical Instrument Co., Ltd. — Class I — 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 | 69756108002500YQ | Class I | Active |
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Manufacturer
- Manufacturer
- Changzhou Centrau Medical Instrument Co., Ltd.
- EUDAMED SRN
- CN-MF-000027491
- Authorised Representative
- phoenix Medtech GmbH DE-AR-000007996
Sources (1)
- EUDAMED 3a70115e-98e8-4785-a452-414bd7f00532 61 fields · synced Jun 19, 2026