Vive LVA1038PAK3
Vive LVA1038PAK3 is a Class I device made by Vive Health LLC, listed in FDA GUDID since 17 Jul 2024 (UDI-DI 00810113578262), 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 | Number00810113578262 | Date17 Jul 2024 | StatusListed |
Official records
- AccessGUDID record 00810113578262
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vive
- Generic name
- Commode, manual
- Model / reference
- LVA1038PAK3
- Primary DI / UDI-DI
- 00810113578262
- FDA product code
- ILS
- GMDN term
- Commode, manual
- Device class
- Class I
- Regulation number
- 890.5050
- GUDID distribution status
- In Commercial Distribution
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