don kelly dissection forceps - PMDA ID 790130_13B3X10305EG7099_A_01_01
Access comprehensive regulatory information for don kelly dissection forceps (ドン・ケリー剥離鉗子) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 790130_13B3X10305EG7099_A_01_01 and manufactured by Manufacture and sales/Sunmedics Co., Ltd.. The device information was last updated on May 11, 2022.
This page provides complete registration details including device class (A3900), classification (pliers / 鉗子), manufacturer information (English and Japanese), intended use, and regulatory compliance data from the official Japan PMDA medical device database. Pure Global AI offers free bilingual access to Japan's complete medical device registry, helping global MedTech companies navigate PMDA regulations efficiently.
This product is a surgical instrument used to grip, bind, compress or support an organ, tissue or blood vessel atraumatically. This product can be reused.
本 製品は、臓器、組織又は血管を非外傷的に把持、結合、圧迫又は支持するために用いる手術器械である。なお、本品は再使用可能である。