Sunny Medical Device (Shenzhen) Co., Ltd.
Country not established FDA establishment FEI 3007361214
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Sunmed Disposable Angio-Closure Pads Ref K191827
Regimes: 510(k) Registry: 510(k)Summed High Pressure Line Ref K140356
Regimes: 510(k) Registry: 510(k)Sunmed Haemostatic Valves Ref K153685
Regimes: 510(k) Registry: 510(k)Sunmed Control Syringes Ref K160190
Regimes: 510(k) Registry: 510(k)Sunmed Guide Wire Ref K120119
Regimes: 510(k) Registry: 510(k)Summed Inflation Device Kit Ref K133795
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3007361214
- Address
- 1/F, Zhongtianxin Building B, Shenzhen Guangdong
Frequently asked questions
How many devices does SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD. have in the registry?
The registry currently lists 6 devices for SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.'s devices?
Among its 6 most recently registered devices, SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD. has devices listed in FDA 510(k) (6 devices).
What risk classes do SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD. in the registry?
The most recently registered devices listed for SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD. include Sunmed Disposable Angio-Closure Pads, SUMMED HIGH PRESSURE LINE, Sunmed Haemostatic Valves and Sunmed Control Syringes.