Anrei Medical (Hangzhou) Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Anrei Medical (Hangzhou) Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Multi-Functional Electrosurgical Knife, Single Use Injection Needle, Rescue Pulmonary Grasping Forceps
6
Total
6
Cleared
0
Denied
Anrei Medical (Hangzhou) Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Hangzhou, CN.
Last cleared in 2022. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Anrei Medical (Hangzhou) Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Beijing Believe-Med Technology Service Co., Ltd. and Boston Scientific Corporation.
FDA 510(k) Regulatory Record - Anrei Medical (Hangzhou) Co., Ltd.
6 devices
Cleared
Mar 21, 2022
Multi-Functional Electrosurgical Knife
Gastroenterology & Urology
182d
Cleared
May 28, 2021
Single Use Injection Needle
Gastroenterology & Urology
60d
Cleared
Apr 29, 2021
Rescue Pulmonary Grasping Forceps
Anesthesiology
211d
Cleared
Apr 27, 2021
Stone Retrieval Balloon Catheter
Gastroenterology & Urology
54d
Cleared
Oct 19, 2020
Single Use Rotatable and Repositionable Hemoclip
Gastroenterology & Urology
112d
Cleared
May 14, 2020
Single Use Endoscope Valves Set
Gastroenterology & Urology
288d