Taiwan FDA registration f8cabd7d412a66ab73adf241fa53e73c
"FertiPro" Media for Assisted Reproduction
TW: "費提普羅"生殖細胞培養試劑
Taiwan·Risk Class 2·MD·FERTIPRO N.V.·Registered Mar 06, 2017 – Mar 06, 2027ActiveRegistration details
- Analysis ID
- f8cabd7d412a66ab73adf241fa53e73c
- License Form
- Ministry of Health Medical Device Import No. 029403
- Customs Code
- DHA05602940306
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
- Mar 06, 2017
- Expiry Date
- Mar 06, 2027
About this record
Access comprehensive regulatory information for "FertiPro" Media for Assisted Reproduction in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8cabd7d412a66ab73adf241fa53e73c 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