Identity
- Trade Name
- StimuLong Sono II NanoLine FDA UDI
- Generic Name
- Peripheral anaesthesia catheter set, non-medicated FDA UDI
- Device Name
- StimuLong Sono II NanoLine SonoLong NanoLine cannula 18G x 100mm, Tuohy tip and Cornerstone Reflectors FDA UDI
- Model / Reference
- 521187-32C FDA UDI
- Description
- StimuLong Sono II NanoLine SonoLong NanoLine cannula 18G x 100mm, Tuohy tip and Cornerstone Reflectors FDA UDI
Identifiers
- Catalog Number
- 521187-32C FDA UDI
- Primary DI / UDI-DI
- 14048223021740 FDA UDI
- FDA Product Code
- CAZ FDA UDI
- GMDN Term
- Peripheral anaesthesia catheter set, non-medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5140 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
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
MR Unsafe FDA UDI
StimuLong Sono II NanoLine 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 d9cba01d-7fa5-44f1-8d62-32a24ea4ab31 36 fields · synced Jun 1, 2026