Data / Medical devices / Irradiator, Blood To Prevent Graft Versus Host Disease
Irradiator, Blood To Prevent Graft Versus Host Disease (MOT): 4 FDA-registered makers in 4 countries
4 establishments in 4 countries are registered with the FDA to make Irradiator, Blood To Prevent Graft Versus Host Disease (product code MOT, Class U). 3 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 16 510(k) clearances under this code, the latest on August 17, 2020, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MOT
- Device class
- U
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| Canada | 1 |
| Italy | 1 |
| United States | 1 |
| China | 1 |
Makers of Irradiator, Blood To Prevent Graft Versus Host Disease
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Best Theratronics Ltd. | Kanata Ontario, Canada | Manufacturer | 3 | January 2, 2019 | 0 | 1 | 0 | api.fda.gov |
| Gilardoni S.P.A. | MANDELLO DEL LARIO Lecco, Italy | Manufacturer | 1 | August 17, 2020 | 0 | 0 | 0 | api.fda.gov |
| Rad Source Technologies, Inc. | Buford, GA, United States | Manufacturer | 1 | February 17, 2009 | 0 | 1 | 0 | api.fda.gov |
| Rad Source(china) Medical Technologies Company Limited | Weihai Shandong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 17, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.