Zibo Hengde Plastic & Rubber Products Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 2
What Zibo Hengde Plastic & Rubber Products Co., Ltd. makes
The company manufactures powder-free and powdered vinyl patient examination gloves, designed for single-use clinical and medical procedures to maintain hygiene and reduce contamination risk during patient care.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Powder-Free Vinyl Patient Examination Gloves Ref K070006
Regimes: 510(k) Registry: 510(k)Powdered Vinyl Patient Examination Gloves Ref K070008
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Zibo Hengde Plastic & Rubber Products Co., Ltd. have in the registry?
The registry currently lists 2 devices for Zibo Hengde Plastic & Rubber Products Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zibo Hengde Plastic & Rubber Products Co., Ltd.'s devices?
Among its 2 most recently registered devices, Zibo Hengde Plastic & Rubber Products Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Zibo Hengde Plastic & Rubber Products Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Zibo Hengde 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 Hengde Plastic & Rubber Products Co., Ltd. in the registry?
The most recently registered devices listed for Zibo Hengde Plastic & Rubber Products Co., Ltd. include POWDER-FREE VINYL PATIENT EXAMINATION GLOVES and POWDERED VINYL PATIENT EXAMINATION GLOVES.