Huizhou Jie Bai Purification Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Huizhou Jie Bai Purification Co., Ltd. makes
Huizhou Jie Bai Purification Co., Ltd. manufactures medical face masks, including the model MY020003, designed for respiratory protection in clinical and healthcare settings.
The company’s products are classified as Class II devices under FDA regulations and are listed in the FDA’s 510(k) premarket notification database. The manufacturer is based in the United States.
Catalogue
Medical Face Masks, Model Name:MY020003 Ref K211165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Huizhou Jie Bai Purification Co., Ltd. have in the registry?
The registry currently lists 1 device for Huizhou Jie Bai Purification Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Huizhou Jie Bai Purification Co., Ltd.'s devices?
Among its 1 most recently registered device, Huizhou Jie Bai Purification Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Huizhou Jie Bai Purification Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Huizhou Jie Bai Purification Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Huizhou Jie Bai Purification Co., Ltd. in the registry?
The most recently registered devices listed for Huizhou Jie Bai Purification Co., Ltd. include Medical Face Masks, Model Name:MY020003.