Taiwan FDA registration 202f3e92bc446b1b7e5c0c261e57dc75
"Addomon" neonatal phototherapy device
TW: “亞多蒙”新生兒光照治療裝置
Registration details
- Analysis ID
- 202f3e92bc446b1b7e5c0c261e57dc75
- Customs Code
- DHA00602484902
Company information
- Manufacturer
- Atom Medical Corporation Urawa Factory
- Manufacturer Country
- Japan
- Authorized Representative
- PROMED INSTRUMENT CO., 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)
- J.5700 Neonatal light therapy device
- Import Information
- import
Dates and status
- Registration Date
- Apr 12, 2013
- Expiry Date
- Apr 12, 2028
About this record
Access comprehensive regulatory information for "Addomon" neonatal phototherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 202f3e92bc446b1b7e5c0c261e57dc75 and manufactured by Atom Medical Corporation Urawa Factory. The authorized representative in Taiwan is PROMED INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices