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“Jeisys” Phototherapy Unit - Taiwan Registration 3f3f2ddff33b5307b446aef5090e2944

Access comprehensive regulatory information for “Jeisys” Phototherapy Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f3f2ddff33b5307b446aef5090e2944 and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is Taike Medical Technology Co.,Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Jeisys Medical Inc., and 3 recent registrations in the same category. 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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3f3f2ddff33b5307b446aef5090e2944
Registration Details
Taiwan FDA Registration: 3f3f2ddff33b5307b446aef5090e2944
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Device Details

“Jeisys” Phototherapy Unit
TW: “婕希”光療儀
Risk Class 2
MD

Registration Details

3f3f2ddff33b5307b446aef5090e2944

Ministry of Health Medical Device Import No. 032690

DHA05603269006

Company Information

Korea, Republic of

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Jun 17, 2019

Jun 17, 2024

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