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“GE” BiliSoft phototherapy System - Taiwan Registration fe00e5880a642d6fe415d8cf6b8e94dd

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 fe00e5880a642d6fe415d8cf6b8e94dd and manufactured by Lumitex Medical Devices, 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, 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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fe00e5880a642d6fe415d8cf6b8e94dd
Registration Details
Taiwan FDA Registration: fe00e5880a642d6fe415d8cf6b8e94dd
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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

fe00e5880a642d6fe415d8cf6b8e94dd

Ministry of Health Medical Device Import No. 034264

DHA05603426402

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

Jan 17, 2021

Jan 17, 2026

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