Tianjin Medis Medical Device Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Tianjin Medis Medical Device Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Endotracheal Tube, Accucuff Cuff Pressure Indicator, Disposable Endotracheal tube, sterile, AccuCuff
3
Total
3
Cleared
0
Denied
Tianjin Medis Medical Device Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Tianjin City, CN.
Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Tianjin Medis Medical Device Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mid-Link Consulting Co, Ltd. and Osmunda Medical Device Consulting Co., Ltd..
FDA 510(k) Regulatory Record - Tianjin Medis Medical Device Co., Ltd.
3 devices