“GE” BiliSoft phototherapy System
Taiwan·Risk Class 2·MD·Lumitex Medical Devices, Inc.·Registered Jan 17, 2021 – Jan 17, 2026Expired- Analysis ID
- fe00e5880a642d6fe415d8cf6b8e94dd
- License Form
- Ministry of Health Medical Device Import No. 034264
- Customs Code
- DHA05603426402
- Manufacturer
- Lumitex Medical Devices, 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
- Jan 17, 2021
- Expiry Date
- Jan 17, 2026
Top companies providing products similar to "“GE” BiliSoft phototherapy System"
Recently registered similar products
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.