“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.
Device Details
Registration Details
1fed2922608ae078d10d9767de970231
Ministry of Health Medical Device Import No. 029239
DHA05602923906
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

