Taiwan FDA registration 1fed2922608ae078d10d9767de970231

“GE” BiliSoft phototherapy system

TW: “奇異”新生兒光照射治療裝置
Taiwan flagTaiwan·Risk Class 2·MD·Lumitex, Inc·Registered Dec 30, 2016 – Dec 30, 2021Expired
Registration details
Analysis ID
1fed2922608ae078d10d9767de970231
License Form
Ministry of Health Medical Device Import No. 029239
Customs Code
DHA05602923906
Company information
Manufacturer
Lumitex, Inc
Manufacturer Country
United States
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J5700 Neonatal Light Irradiation Therapy Device
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 30, 2016
Expiry Date
Dec 30, 2021
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About this record

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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