VIPER PRIME instrument set
- Device Type
- MD
- Device Class
- A5800
- Class Name (English)
- Instruments for spine surgery
- Class Name (日本語)
- 脊椎手術用器械
- PMDA ID
- 340216_13B1X00204DS0066_A_01_02
- Last Update Date
- August 09, 2022
- Official Documents
- View PDF (PMDA)
- English
- Johnson & Johnson K.K.
- 日本語 (Japanese)
- 製造販売/ジョンソン・エンド・ジョンソン株式会社
Access comprehensive regulatory information for VIPER PRIME instrument set (VIPER PRIME 器械セット) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340216_13B1X00204DS0066_A_01_02 and manufactured by Johnson & Johnson K.K.. The device information was last updated on August 09, 2022.
This page provides complete registration details including device class (A5800), classification (Instruments for spine surgery / 脊椎手術用器械), 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.