Fatrotek S.r.l.
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Fatrotek S.r.l. makes
Fatrotek S.R.L. manufactures the RUGALIFT (Model V.2.1), a patient transfer device designed to assist healthcare providers in safely moving patients between surfaces, such as beds and wheelchairs, while reducing physical strain.
The RUGALIFT is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Rugalift, Model# V.2.1 Ref K071573
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fatrotek S.R.L. have in the registry?
The registry currently lists 1 device for Fatrotek S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fatrotek S.R.L.'s devices?
Among its 1 most recently registered device, Fatrotek S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Fatrotek S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fatrotek S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fatrotek S.R.L. in the registry?
The most recently registered devices listed for Fatrotek S.R.L. include RUGALIFT, MODEL# V.2.1.