Identity
- Trade Name
- NeuroFlex FDA UDI
- Generic Name
- Eye-tracking neurological/brain injury assessment device FDA UDI
- Model / Reference
- NeuroFlex FDA UDI
Identifiers
- Primary DI / UDI-DI
- G676NEUROFLEX0 FDA UDI
- FDA Product Code
- PTY FDA UDI
- GMDN Term
- Eye-tracking neurological/brain injury assessment device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1470 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye-tracking neurological/brain injury assessment device
NeuroFlex by Saccade Analytiques Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye-tracking neurological/brain injury assessment device.
- EyeBOX — OCULOGICA INC. · Class II
- EYE-SYNC — NEUROSYNC, INC. · 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
- Saccade Analytiques Inc
Sources (1)
- FDA UDI dec355c3-162b-49b7-9378-4f80baa9fe31 32 fields · synced Jun 8, 2026