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“Tokyo Iken” Super Lizer Near-Infrared therapy device - Taiwan Registration b096ccef28192064c5e425d122f6950c

Access comprehensive regulatory information for “Tokyo Iken” Super Lizer Near-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 b096ccef28192064c5e425d122f6950c and manufactured by TOKYO IKEN CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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b096ccef28192064c5e425d122f6950c
Registration Details
Taiwan FDA Registration: b096ccef28192064c5e425d122f6950c
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Device Details

“Tokyo Iken” Super Lizer Near-Infrared therapy device
TW: “東京醫研”近紅外線治療儀
Risk Class 2
MD

Registration Details

b096ccef28192064c5e425d122f6950c

Ministry of Health Medical Device Import No. 031240

DHA05603124009

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

o Equipment for physical medicine

O5500 infrared light

Imported from abroad

Dates and Status

Aug 10, 2018

Aug 10, 2028