Identity
- Trade Name
- NeuralBot Procedural Set (Single Use) FDA UDI
- Generic Name
- Noninvasive vascular ultrasound support kit FDA UDI
- Device Name
- The NeuralBot procedural set contains the following single use items; probe pod covers, head cradle comfort padding, head stabilizer comfort padding, and registration dots. FDA UDI
- Model / Reference
- 1.x FDA UDI
- Description
- The NeuralBot procedural set contains the following single use items; probe pod covers, head cradle comfort padding, head stabilizer comfort padding, and registration dots. FDA UDI
Identifiers
- Catalog Number
- NA-DSP2 FDA UDI
- Primary DI / UDI-DI
- 00850681007115 FDA UDI
- 510(k) Number
- K180455 FDA UDI
- FDA Product Code
- ITX FDA UDIOQQ FDA UDIIYN FDA UDI
- GMDN Term
- Noninvasive vascular ultrasound support kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1570 FDA UDI892.1550 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
FDA UDI
NeuralBot Procedural Set (Single Use) by Novasignal Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Novasignal Corporation
Sources (1)
- FDA UDI c000d675-321a-4bdb-b446-a50e56e173a6 36 fields · synced May 30, 2026