Japan PMDA registration 130152_13B1X00048002426_1_01_01

DIAMATRIX I/A chip

JP: DIAMATRIX I/A チップ
Japan flagJapan·MD·A4701·Updated June 16, 2022
Intended use / 使用目的
English
A tubular device used for injecting perfusion fluid and aspiration of intraocular substances during eye surgery.
日本語 (Japanese)
眼科手術時に灌流液などの注入及び眼内物質の吸引に使用する筒状の機器。
Device classification / 分類
Device Type
MD
Device Class
A4701
Class Name (English)
reusable eye surgery cannula
Class Name (日本語)
再使用可能な眼科手術用カニューレ
Registration information / 登録情報
PMDA ID
130152_13B1X00048002426_1_01_01
Last Update Date
June 16, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社イナミ
About this record

Access comprehensive regulatory information for DIAMATRIX I/A chip (DIAMATRIX I/A チップ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 130152_13B1X00048002426_1_01_01 and manufactured by Inami Co., Ltd.. The device information was last updated on June 16, 2022.

This page provides complete registration details including device class (A4701), classification (reusable eye surgery cannula / 再使用可能な眼科手術用カニューレ), 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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