Shijiazhuang Benestar Plastic Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shijiazhuang Benestar Plastic Co., Ltd. have in the registry?
The registry currently lists 1 device for Shijiazhuang Benestar Plastic Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shijiazhuang Benestar Plastic Co., Ltd.'s devices?
Among its 1 most recently registered device, Shijiazhuang Benestar Plastic Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Shijiazhuang Benestar Plastic Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shijiazhuang Benestar Plastic Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Shijiazhuang Benestar Plastic Co., Ltd. in the registry?
The most recently registered devices listed for Shijiazhuang Benestar Plastic Co., Ltd. include POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED).