Japan PMDA registration 530150_22300BZX00040000_A_01_07

Nexload System SP

JP: ネックスロードシステム SP
Japan flagJapan·MD·A7200·Updated May 27, 2024
Device classification / 分類
Device Type
MD
Device Class
A7200
Class Name (English)
Post-chamber lens with insertion device
Class Name (日本語)
挿入器付後房レンズ
Registration information / 登録情報
PMDA ID
530150_22300BZX00040000_A_01_07
Last Update Date
May 27, 2024
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社ニデック
About this record

Access comprehensive regulatory information for Nexload System SP (ネックスロードシステム SP) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530150_22300BZX00040000_A_01_07 and manufactured by NIDEK Corporation. The device information was last updated on May 27, 2024.

This page provides complete registration details including device class (A7200), classification (Post-chamber lens with insertion device / 挿入器付後房レンズ), 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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