Cable ready needle cable titanium alloy - PMDA ID 340772_21200BZY00318000_A_01_06
Access comprehensive regulatory information for Cable ready needle cable titanium alloy (ケーブルレディー ニードルケーブル チタン合金) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340772_21200BZY00318000_A_01_06 and manufactured by Manufacture and sales/Zimmer Biomet LLC. The device information was last updated on March 29, 2022.
This page provides complete registration details including device class (A5800), classification (internal fixation cable / 体内固定用ケーブル), 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 an implant used in orthopedics for reduction fixation at the time of fracture of the olecranon, patella, femur, humerus and tarsal joint. In addition, since it is sterile, it can be used immediately as it is.
本品は整形外科において肘頭、膝蓋骨、大腿骨、上腕骨及び足根関節部等の骨折時の整復固定に用いられるインプラントである。又、滅菌済みであるのでそのまま直ちに使用できる。