Identity
- Trade Name
- Vector Elite FDA UDI
- Generic Name
- Gait rehabilitation frame, electric FDA UDI
- Device Name
- Vector Gait and Safety System FDA UDI
- Model / Reference
- VEC-1000 FDA UDI
- Description
- Vector Gait and Safety System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815962020269 FDA UDI
- FDA Product Code
- BXB FDA UDI
- GMDN Term
- Gait rehabilitation frame, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5380 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Gait rehabilitation frame, electric
Vector Elite by Bioness Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Gait rehabilitation frame, electric.
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- SafeGait Active 360 Dynamic Mobility Trainer — DIH TECHNOLOGY INC. · Class I
- Healing Innovations — HEALING INNOVATIONS · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Bioness Inc.
Sources (1)
- FDA UDI 7820fdeb-f6ae-4c68-b122-8f790ca948f4 35 fields · synced Jun 8, 2026