Identity
- Trade Name
- SonoBlock II Facet FDA UDI
- Generic Name
- Peripheral nerve-block sharp needle FDA UDI
- Device Name
- SonoBlock II Facet 22G (0,70) x 50mm with injection tube FDA UDI
- Model / Reference
- 001280-74 FDA UDI
- Description
- SonoBlock II Facet 22G (0,70) x 50mm with injection tube FDA UDI
Identifiers
- Catalog Number
- 001280-74 FDA UDI
- Primary DI / UDI-DI
- 14048223033170 FDA UDI
- FDA Product Code
- BSP FDA UDI
- GMDN Term
- Peripheral nerve-block sharp needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5150 FDA UDI
- Commercial Distribution
- Not 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
No
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
No
FDA UDI
MR Unsafe FDA UDI
SonoBlock II Facet by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Pajunk GmbH Medizintechnologie
Sources (1)
- FDA UDI 780e0a23-be23-4dc3-8c36-581779957048 36 fields · synced Jun 1, 2026