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“GE” BiliSoft phototherapy system - Taiwan Registration 1fed2922608ae078d10d9767de970231

Access comprehensive regulatory information for “GE” BiliSoft phototherapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fed2922608ae078d10d9767de970231 and manufactured by Lumitex, Inc. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Lumitex Medical Devices, Inc., and 1 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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1fed2922608ae078d10d9767de970231
Registration Details
Taiwan FDA Registration: 1fed2922608ae078d10d9767de970231
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Device Details

“GE” BiliSoft phototherapy system
TW: “奇異”新生兒光照射治療裝置
Risk Class 2
MD

Registration Details

1fed2922608ae078d10d9767de970231

Ministry of Health Medical Device Import No. 029239

DHA05602923906

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J5700 Neonatal Light Irradiation Therapy Device

Imported from abroad

Dates and Status

Dec 30, 2016

Dec 30, 2021

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