Japan PMDA registration 340216_13B1X00204DS0066_A_01_02

VIPER PRIME instrument set

JP: VIPER PRIME 器械セット
Japan flagJapan·MD·A5800·Updated August 09, 2022
Device classification / 分類
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
Registration information / 登録情報
PMDA ID
340216_13B1X00204DS0066_A_01_02
Last Update Date
August 09, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
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
About this record

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.

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