Rossmax Internationl, Ltd.
TaiwanFDA applicant, unverified
- Devices
- 4
Catalogue
Wristwatch Blood Pressure Monitor, Model A43 Ref K010190
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Wristwatch Blood Pressure Monitor A46 Ref K010498
Regimes: 510(k) Registry: 510(k)Rossmax Digital Sphygmomanometer Mandaus Ii Ref K053006
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rossmax Internationl, Ltd. have in the registry?
The registry currently lists 4 devices for Rossmax Internationl, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rossmax Internationl, Ltd.'s devices?
Among its 4 most recently registered devices, Rossmax Internationl, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Rossmax Internationl, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Rossmax Internationl, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rossmax Internationl, Ltd. in the registry?
The most recently registered devices listed for Rossmax Internationl, Ltd. include WRISTWATCH BLOOD PRESSURE MONITOR, MODEL A43, ROSSMAX AUTOMATIC WRIST BLOOD PRESSURE MONITOR, MODELS B150 & Q400, WRISTWATCH BLOOD PRESSURE MONITOR A46 and ROSSMAX DIGITAL SPHYGMOMANOMETER MANDAUS II.