Identity
- Trade Name
- Vector Base FDA UDI
- Generic Name
- Gait rehabilitation frame, manual FDA UDI
- Device Name
- Vector Gait and Safety System, Base Model FDA UDI
- Model / Reference
- VEC-3000 FDA UDI
- Description
- Vector Gait and Safety System, Base Model FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810188050557 FDA UDI
- FDA Product Code
- ION FDA UDI
- GMDN Term
- Gait rehabilitation frame, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5370 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Gait rehabilitation frame, manual
Vector Base by Bioness Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Gait rehabilitation frame, manual.
- Vector Base — BIONESS INC. · 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 |
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Manufacturer
- Manufacturer
- Bioness Medical, Inc.
Sources (1)
- FDA UDI 433eb6be-f2d3-44b1-9ef5-6a98a46afb55 34 fields · synced Jun 9, 2026