Identity
- Trade Name
- Neurosign V4 FDA UDI
- Generic Name
- Nerve-locating system probe, single-use FDA UDI
- Device Name
- Diposable Curved Needles, 167mm stimulating electrode and 14mm x 0,38mm needle electrode FDA UDI
- Model / Reference
- 4016-00 FDA UDI
- Description
- Diposable Curved Needles, 167mm stimulating electrode and 14mm x 0,38mm needle electrode FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08718375865972 FDA UDI
- FDA Product Code
- ETN FDA UDI
- GMDN Term
- Nerve-locating system probe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.1820 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
Yes
FDA UDI
Neurosign V4 by Technomed Engineering B.V. — 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
- Technomed Engineering B.V.
Sources (1)
- FDA UDI f4fb681a-0f81-4677-8caa-a7a672193068 35 fields · synced May 31, 2026