Identity
- Trade Name
- NerveGuard FDA UDI
- Generic Name
- Nerve-block injection manometer FDA UDI
- Device Name
- NerveGuard Injection pressure device for cannulas 18-22G FDA UDI
- Model / Reference
- 001151-38M FDA UDI
- Description
- NerveGuard Injection pressure device for cannulas 18-22G FDA UDI
Identifiers
- Catalog Number
- 001151-38M FDA UDI
- Primary DI / UDI-DI
- 04048223069608 FDA UDI
- 510(k) Number
- K170435 FDA UDI
- FDA Product Code
- BSP FDA UDI
- GMDN Term
- Nerve-block injection manometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5150 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
No
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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Nerve-block injection manometer
NerveGuard by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nerve-block injection manometer.
- B-Smart — HMC PREMEDICAL SPA · Class II
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 39e95e26-2bdb-469e-8716-6a131f4104b9 37 fields · synced May 31, 2026