Vector Base VEC-3000
by Bioness Inc.
Vector Base VEC-3000 is a Class I device made by Bioness Inc., listed in FDA GUDID since 7 Dec 2017 (UDI-DI 00815962020283), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00815962020283 | Date7 Dec 2017 | StatusListed |
Official records
- AccessGUDID record 00815962020283
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vector Base
- Generic name
- Gait rehabilitation frame, manual
- Model / reference
- VEC-3000
- Primary DI / UDI-DI
- 00815962020283
- FDA product code
- IKX
- GMDN term
- Gait rehabilitation frame, manual
- Device class
- Class I
- Regulation number
- 890.5050
- GUDID distribution status
- In Commercial Distribution
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