Aqua 3.2
Aqua 3.2 is a Class I device made by Elekta Solutions AB, listed in FDA GUDID since 15 May 2025 (UDI-DI 07340201500101), 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 | Number07340201500101 | Date15 May 2025 | StatusListed |
Official records
- AccessGUDID record 07340201500101
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aqua
- Generic name
- Radiation therapy software
- Model / reference
- AQUA 3.2
- Primary DI / UDI-DI
- 07340201500101
- FDA product code
- LHO
- GMDN term
- Radiation therapy software
- Device class
- Class I
- Regulation number
- 892.1940
- GUDID distribution status
- In Commercial Distribution
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