Zhonghong Pulin Medical Products Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3010201834
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
- Authorised rep.
- Lotus NL B.V.NL
Catalogue
- Registry: GUDID
- Registry: GUDID
- Regimes: CE MDR 510(k) Registry: 510(k)
NitriTec Vinyl Glove Powder Free Blue Ref K210460
Regimes: 510(k) Registry: 510(k)- Regimes: CE MDR 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010201834
- DUNS number
- 548208657
- Address
- West Industrial Park, BDA, Luannan County, Tangshan Hebei
Frequently asked questions
How many devices does Zhonghong Pulin Medical Products Co., Ltd. have in the registry?
The registry currently lists 5 devices for Zhonghong Pulin Medical Products Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zhonghong Pulin Medical Products Co., Ltd.'s devices?
Among its 5 most recently registered devices, Zhonghong Pulin Medical Products Co., Ltd. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Zhonghong Pulin Medical Products Co., Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Zhonghong Pulin Medical Products Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zhonghong Pulin Medical Products Co., Ltd. in the registry?
The most recently registered devices listed for Zhonghong Pulin Medical Products Co., Ltd. include ZHONGHONG PULIN S, Nitrile Exam Glove, Tested For Use With Chemotherapy Drugs And Fentanyl, NitriTec Vinyl Glove Powder Free Blue and Nitrile Exam Glove, Extended cuff, Tested For Use With Chemotherapy Drugs, Fentanyl Citrate, And Select Other Drugs.