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Root Retractor
EUDAMEDClass I (EU MDR)
Ref N/AModel UBE-A-xxxx-xxxx、UBE-FD-xxxx-xxxx
Identity
- Device Name
- Root Retractor EUDAMED
- Model / Reference
- UBE-A-xxxx-xxxx、UBE-FD-xxxx-xxxx EUDAMEDN/A EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06942455433580 EUDAMED
- Basic UDI-DI
- 69271553BONSS1646Y EUDAMED
- Direct Marketing DI
- 06942455433580 EUDAMED
- EMDN Code
- L0908 ORTHOPAEDIC AND TRAUMATOLOGICAL TRACTION INSTRUMENTS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria 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
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Root Retractor by Jiangsu Bonss Medical Technology 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 | 69271553BONSS1646Y | Class I | Active |
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Manufacturer
- Manufacturer
- Jiangsu Bonss Medical Technology Co Ltd
- EUDAMED SRN
- CN-MF-000023743
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED dee570fa-de6c-4acd-afe7-bacfcce0afe1 61 fields · synced Jun 19, 2026