Identity
- Trade Name
- NuMED, Inc. Bonhoeffer FDA UDI
- Generic Name
- Peripheral vascular guidewire, manual FDA UDI
- Model / Reference
- J3FC-SS C 210-035 FDA UDI
Identifiers
- Catalog Number
- RM0279-01 FDA UDI
- Primary DI / UDI-DI
- 10887714024532 FDA UDI
- FDA Product Code
- DQX FDA UDI
- GMDN Term
- Peripheral vascular guidewire, manual FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1330 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Peripheral vascular guidewire, manual
NuMED, Inc. Bonhoeffer by Lake Region Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Lake Region Medical Limited
Sources (1)
- FDA UDI c7400de2-7235-4d1c-a7a3-1f636955f1e3 34 fields · synced Jun 8, 2026