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“Jeisys” Therapeutical Laser Unit - Taiwan Registration e5b9d181f4e3d5b3cbba180414890ced

Access comprehensive regulatory information for “Jeisys” Therapeutical Laser Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5b9d181f4e3d5b3cbba180414890ced and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..

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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e5b9d181f4e3d5b3cbba180414890ced
Registration Details
Taiwan FDA Registration: e5b9d181f4e3d5b3cbba180414890ced
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Device Details

“Jeisys” Therapeutical Laser Unit
TW: “樂福”雷射治療儀
Risk Class 2
MD

Registration Details

e5b9d181f4e3d5b3cbba180414890ced

Ministry of Health Medical Device Import No. 032900

DHA05603290004

Company Information

Korea, Republic of

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

Oct 21, 2019

Oct 21, 2024