Taiwan FDA registration 0f94b1331c3aab769df1664e84d0b958
“FertiPro” Media for Micromanipulation
TW: “費提普羅”顯微操作試劑
Taiwan·Risk Class 2·MD·FERTIPRO N.V.·Registered Aug 07, 2020 – Aug 07, 2025ExpiredRegistration details
- Analysis ID
- 0f94b1331c3aab769df1664e84d0b958
- License Form
- Ministry of Health Medical Device Import No. 033878
- Customs Code
- DHA05603387803
Company information
- Manufacturer
- FERTIPRO N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- ESSENCE EQUIP CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6180 Reproductive vehicles and supplements
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 07, 2020
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for “FertiPro” Media for Micromanipulation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f94b1331c3aab769df1664e84d0b958 and manufactured by FERTIPRO N.V.. The authorized representative in Taiwan is ESSENCE EQUIP 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