Ria Tech Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Ria Tech Co., Ltd. makes
Ria Tech Co., Ltd. manufactures the RIA Safeguard, a medical device designed for patient monitoring or safety applications within healthcare settings.
The RIA Safeguard is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
RIA Safeguard Ref K222416
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ria Tech Co., Ltd. have in the registry?
The registry currently lists 1 device for Ria Tech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ria Tech Co., Ltd.'s devices?
Among its 1 most recently registered device, Ria Tech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ria Tech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ria Tech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ria Tech Co., Ltd. in the registry?
The most recently registered devices listed for Ria Tech Co., Ltd. include RIA Safeguard.