Xinaomdt Technology Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Xinaomdt Technology Co., Ltd. makes
Xinaomdt Technology Co., Ltd. manufactures the MSTAR MPD4500, a medical device designed for diagnostic or therapeutic use in a specialized clinical setting, though the exact application is not specified in the provided data.
The MSTAR MPD4500 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Mstar MPD4500 Ref K073457
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Xinaomdt Technology Co., Ltd. have in the registry?
The registry currently lists 1 device for Xinaomdt Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xinaomdt Technology Co., Ltd.'s devices?
Among its 1 most recently registered device, Xinaomdt Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Xinaomdt Technology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Xinaomdt Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xinaomdt Technology Co., Ltd. in the registry?
The most recently registered devices listed for Xinaomdt Technology Co., Ltd. include MSTAR MPD4500.