Safetech Intl., Inc.
Country not established
- Devices
- 1
What Safetech Intl., Inc. makes
Safetech Intl., Inc. manufactures the Doyle Extractor, a device designed for the removal of foreign bodies or obstructions from the gastrointestinal tract, particularly in pediatric or emergency cases.
The Doyle Extractor is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Doyle Extractor Ref K955748
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Safetech Intl., Inc. have in the registry?
The registry currently lists 1 device for Safetech Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Safetech Intl., Inc.'s devices?
Among its 1 most recently registered device, Safetech Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Safetech Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Safetech Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Safetech Intl., Inc. in the registry?
The most recently registered devices listed for Safetech Intl., Inc. include DOYLE EXTRACTOR.