Taiwan FDA registration b6b059bb8542882c9226d8f84ba18433
“Vitrolife” culture system
TW: “密陀來福”生殖細胞培養系統
Taiwan·Risk Class 2·MD·Vitrolife Sweden AB·Registered Jan 05, 2016 – Jan 05, 2026ExpiredRegistration details
- Analysis ID
- b6b059bb8542882c9226d8f84ba18433
- License Form
- Ministry of Health Medical Device Import No. 028132
- Customs Code
- DHA05602813209
Company information
- Manufacturer
- Vitrolife Sweden AB
- Manufacturer Country
- Sweden
- Authorized Representative
- TSENG HSIANG LIFE SCIENCE 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
- Jan 05, 2016
- Expiry Date
- Jan 05, 2026
About this record
Access comprehensive regulatory information for “Vitrolife” culture system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6b059bb8542882c9226d8f84ba18433 and manufactured by Vitrolife Sweden AB. The authorized representative in Taiwan is TSENG HSIANG LIFE SCIENCE LTD..
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