ActiveAid 1100
ActiveAid 1100 is a Class I device made by Altimate Medical, Inc., listed in FDA GUDID since 18 Nov 2022 (UDI-DI 10858921006192), registry data as of 23 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 | Number10858921006192 | Date18 Nov 2022 | StatusListed |
Official records
- AccessGUDID record 10858921006192
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ActiveAid
- Generic name
- Commode, manual
- Model / reference
- 1100
- Primary DI / UDI-DI
- 10858921006192
- FDA product code
- INN
- GMDN term
- Commode, manual
- Device class
- Class I
- Regulation number
- 890.3100
- GUDID distribution status
- In Commercial Distribution
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