Japan PMDA registration 340772_21200BZY00318000_A_01_06

Cable ready needle cable titanium alloy

JP: ケーブルレディー ニードルケーブル チタン合金
Japan flagJapan·MD·A5800·Updated March 29, 2022
Intended use / 使用目的
English
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.
日本語 (Japanese)
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。
Device classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
internal fixation cable
Class Name (日本語)
体内固定用ケーブル
Registration information / 登録情報
PMDA ID
340772_21200BZY00318000_A_01_06
Last Update Date
March 29, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ジンマー・バイオメット合同会社
About this record

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.

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