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Iatro LD-IF (65292-2/65293-9) - PMDA ID 730056_13E1X80073000043_A_01_02

イアトロ LD−IF(65292-2/65293-9)

Access comprehensive regulatory information for Iatro LD-IF (65292-2/65293-9) (イアトロ LD−IF(65292-2/65293-9)) in the Japan medical device market through Pure Global AI's free bilingual database. This IVD medical device is registered under PMDA ID 730056_13E1X80073000043_A_01_02 and manufactured by PHC Corporation. The device information was last updated on February 01, 2025.

This page provides complete registration details including device class (IVD), classification (Lactate dehydrogenase kit / 乳酸脱水素酵素キット), 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.

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PMDA Official Data
Bilingual (EN/JP)
IVD
IVD
730056_13E1X80073000043_A_01_02
IVD
IVD
Iatro LD-IF (65292-2/65293-9)
イアトロ LD−IF(65292-2/65293-9)
PMDA ID: 730056_13E1X80073000043_A_01_02
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Device Classification / 分類
Device Type
IVD
Device Class
IVD
Class Name (English)
Lactate dehydrogenase kit
Class Name (日本語)
乳酸脱水素酵素キット
Registration Information / 登録情報
PMDA ID
730056_13E1X80073000043_A_01_02
Last Update Date
February 01, 2025
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/PHC株式会社
Product Names / 製品名
Market Name (English)
Iatro LD-IF (65292-2/65293-9)
Market Name (日本語)
イアトロ LD−IF(65292-2/65293-9)