surgical kit
Japan·MD·B0200·Updated December 26, 2020- Device Type
- MD
- Device Class
- B0200
- Class Name (English)
- Single-use class III treatment kit
- Class Name (日本語)
- 単回使用クラスIII処置キット
- PMDA ID
- 530780_21500BZZ00504000_C_01_02
- Last Update Date
- December 26, 2020
- Official Documents
- View PDF (PMDA)
- 日本語 (Japanese)
- 製造販売／日本メディカルプロダクツ株式会社
Access comprehensive regulatory information for surgical kit (外科キット) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530780_21500BZZ00504000_C_01_02 and manufactured by Japan Medical Products Co., Ltd.. The device information was last updated on December 26, 2020.
This page provides complete registration details including device class (B0200), classification (Single-use class III treatment kit / 単回使用クラスIII処置キット), manufacturer information (English and Japanese), 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.