Agility™ 1525725
by Elekta Inc.
Agility 1525725 is a medical device (FDA Class II; FDA product code IYE, Accelerator, linear, medical) made by Elekta Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 05060191071031), 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 | Number05060191071031 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 05060191071031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Agility™
- Generic name
- Automatic-aperture-control accelerator system collimator
- Model / reference
- 1525725
- Primary DI / UDI-DI
- 05060191071031
- FDA product code
- IYE
- GMDN term
- Automatic-aperture-control accelerator system collimator
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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