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“Tokyo Iken” Super Lizer mini PRO Infrared therapy device - Taiwan Registration a63087ff0b99611553a64105e052a1a4

Access comprehensive regulatory information for “Tokyo Iken” Super Lizer mini PRO Infrared therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a63087ff0b99611553a64105e052a1a4 and manufactured by TOKYO IKEN CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..

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a63087ff0b99611553a64105e052a1a4
Registration Details
Taiwan FDA Registration: a63087ff0b99611553a64105e052a1a4
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Device Details

“Tokyo Iken” Super Lizer mini PRO Infrared therapy device
TW: “東京醫研” 超萊斯迷你專業版近紅外線治療儀
Risk Class 2
MD

Registration Details

a63087ff0b99611553a64105e052a1a4

Ministry of Health Medical Device Import No. 035123

DHA05603512302

Company Information

Japan

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O5500 infrared light

Imported from abroad

Dates and Status

Dec 27, 2021

Dec 27, 2026