Shanghai Kohope Medical Devices Co., Ltd
Country not established FDA establishment FEI 3009077131
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009077131
- Address
- 1001, Building 2, Lane 2888, SHANGHAI
Frequently asked questions
How many devices does SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD have in the registry?
The registry currently lists 1 device for SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD's devices?
Among its 1 most recently registered device, SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD has devices listed in FDA 510(k) (1 device).
What risk classes do SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD's devices fall under?
Among its 1 most recently registered device, the classes recorded for SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD in the registry?
The most recently registered devices listed for SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD include Sterile Hypodermic Syringe for Single use, with/without needle, Sterile Insulin Syringe for Single use, with needle, Sterile Hypodermic needle for Single use.