Identity
- Trade Name
- VSA-3000 Vibratory Sensory Analazer FDA UDI
- Generic Name
- Vibratory biothesiometer FDA UDI
- Device Name
- The Vibratory Sensory Analyzer VSA-3000 is a computerized device for the quantitative assessment of large nerve fiber dysfunctions, designed for both clinical and advanced research applications. It measures the sensory threshold for vibration. The Device includes: main unit, at least one probe and accessories. FDA UDI
- Model / Reference
- VSA-3000 FDA UDI
- Description
- The Vibratory Sensory Analyzer VSA-3000 is a computerized device for the quantitative assessment of large nerve fiber dysfunctions, designed for both clinical and advanced research applications. It measures the sensory threshold for vibration. The Device includes: main unit, at least one probe and accessories. FDA UDI
Identifiers
- Catalog Number
- MO 00003 FDA UDI
- Primary DI / UDI-DI
- 07290103039004 FDA UDI
- FDA Product Code
- IRO FDA UDI
- GMDN Term
- Vibratory biothesiometer FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5975 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Vibratory biothesiometer
VSA-3000 Vibratory Sensory Analazer by Medoc Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vibratory biothesiometer.
- CASE — WR Medical Electronics Co. · Class I
- NEURO TOUCH — YOSTRA LABS PRIVATE LIMITED · Class I
- VSA 2 Hand-Leg support — Medoc Corp. · Class I
- VSA 2 Handheld device — Medoc Corp. · Class I
- VSA 2 Hand Held — Medoc Corp. · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medoc Corp.
Sources (1)
- FDA UDI c633a197-fd9c-425a-8a98-496f4ed5ed30 34 fields · synced May 31, 2026