Jiangsu Baide Medical Intrument Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Jiangsu Baide Medical Intrument Co., Ltd. makes
Jiangsu Baide Medical Intrument Co., Ltd. makes the Baide device.
The Baide device is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Baide Ref K150009
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jiangsu Baide Medical Intrument Co., Ltd. have in the registry?
The registry currently lists 1 device for Jiangsu Baide Medical Intrument Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jiangsu Baide Medical Intrument Co., Ltd.'s devices?
Among its 1 most recently registered device, Jiangsu Baide Medical Intrument Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Jiangsu Baide Medical Intrument Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jiangsu Baide Medical Intrument Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jiangsu Baide Medical Intrument Co., Ltd. in the registry?
The most recently registered devices listed for Jiangsu Baide Medical Intrument Co., Ltd. include Baide.