Viatro, Corp.
Country not established
- Devices
- 1
What Viatro, Corp. makes
Viatro, Corp. makes the VIRAPUMP II device, including its Models and Model M variants.
The VIRAPUMP II is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Virapump Ii (Models And Model M) Ref K961607
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viatro, Corp. have in the registry?
The registry currently lists 1 device for Viatro, Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viatro, Corp.'s devices?
Among its 1 most recently registered device, Viatro, Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Viatro, Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Viatro, Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viatro, Corp. in the registry?
The most recently registered devices listed for Viatro, Corp. include VIRAPUMP II (MODELS AND MODEL M).