Identity
- Trade Name
- toc1m neurovision transcranial doppler FDA UDI
- Generic Name
- Noninvasive vascular ultrasound system, line-powered FDA UDI
- Device Name
- An electricity (AC-powered) device assembly consisting of a desktop unit, a graphical display unit and an attached probe or interchangeable probes, designed to noninvasively locate and assess the extent of vascular flow restriction (e.g., clots, stenosis, mechanical damage) by measuring blood flow rate using ultrasound/Dopple. Clinical applications include venous/arteria/cardiovascular/cephalic flow screening (e.g., assessment of air embolism, atherosclerosis, varicose veins, venous thrombosis),emboli counting,vasospasm,sah,, and/or blood flow wave form recording. FDA UDI
- Model / Reference
- TOC1M NEUROVISION FDA UDI
- Description
- An electricity (AC-powered) device assembly consisting of a desktop unit, a graphical display unit and an attached probe or interchangeable probes, designed to noninvasively locate and assess the extent of vascular flow restriction (e.g., clots, stenosis, mechanical damage) by measuring blood flow rate using ultrasound/Dopple. Clinical applications include venous/arteria/cardiovascular/cephalic flow screening (e.g., assessment of air embolism, atherosclerosis, varicose veins, venous thrombosis),emboli counting,vasospasm,sah,, and/or blood flow wave form recording. FDA UDI
Identifiers
- Catalog Number
- TOC1M FDA UDI
- Primary DI / UDI-DI
- 08622630003019 FDA UDI
- 510(k) Number
- K060112 FDA UDI
- FDA Product Code
- IYN FDA UDI
- GMDN Term
- Noninvasive vascular ultrasound system, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1550 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Liquid Chemical FDA UDI
Category: Noninvasive vascular ultrasound system, line-powered
toc1m neurovision transcranial doppler by Multigon Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Noninvasive vascular ultrasound system, line-powered.
- Transonic — Transonic Systems Inc. · Class II
- NovaGuide™ Intelligent Ultrasound System — Novasignal Corporation · Class II
- Varia TCD — NEUROCHAOS SOLUTIONS INC · Class II
- Smartdop XT6 — Koven Technology, Inc. · Class II
- Hokanson — D. E. Hokanson, Inc. · Class II
- Sono TT Ultrasonic Flowcomputer — em-tec GmbH · Class II
- Smartdop XT — Koven Technology, Inc. · Class II
- NovaBot Automated Headset — Novasignal Corporation · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Multigon Industries, Inc.
Sources (1)
- FDA UDI e97f3443-ef42-4824-aea6-b8487cc0a371 37 fields · synced Jun 8, 2026