Zibo Borui Plastic & Rubber Products Co., Ltd.
Country not established
- Devices
- 2
What Zibo Borui Plastic & Rubber Products Co., Ltd. makes
Zibo Borui Plastic & Rubber Products Co., Ltd. manufactures disposable powdered vinyl patient examination gloves.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Zibo Borui Plastic & Rubber Products Co., Ltd. have in the registry?
The registry currently lists 2 devices for Zibo Borui Plastic & Rubber Products Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zibo Borui Plastic & Rubber Products Co., Ltd.'s devices?
Among its 2 most recently registered devices, Zibo Borui Plastic & Rubber Products Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Zibo Borui Plastic & Rubber Products Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Zibo Borui Plastic & Rubber Products Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zibo Borui Plastic & Rubber Products Co., Ltd. in the registry?
The most recently registered devices listed for Zibo Borui Plastic & Rubber Products Co., Ltd. include VINYL EXAMINATION GLOVE, POWDER-FREE, NON-STERILE and DISPOSABLE POWDERED VINYL PATIENT EXAMINATION GLOVES.