“GE” BiliSoft phototherapy system
- Analysis ID
- 1fed2922608ae078d10d9767de970231
- License Form
- Ministry of Health Medical Device Import No. 029239
- Customs Code
- DHA05602923906
- Manufacturer
- Lumitex, Inc
- Manufacturer Country
- United States
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- 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
- Registration Date
- Dec 30, 2016
- Expiry Date
- Dec 30, 2021
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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.