Taiwan FDA registration 07b080f5d9a9f7ae0966016a6e61e50c
Vitrolife andrology system
TW: 密陀來福男性生殖培養系統
Taiwan·Risk Class 2·MD·Vitrolife Sweden AB·Registered Jun 13, 2016 – Jun 13, 2026ExpiredRegistration details
- Analysis ID
- 07b080f5d9a9f7ae0966016a6e61e50c
- License Form
- Ministry of Health Medical Device Import No. 028604
- Customs Code
- DHA05602860401
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
- Jun 13, 2016
- Expiry Date
- Jun 13, 2026
About this record
Access comprehensive regulatory information for Vitrolife andrology system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07b080f5d9a9f7ae0966016a6e61e50c and manufactured by Vitrolife Sweden AB. The authorized representative in Taiwan is TSENG HSIANG LIFE SCIENCE LTD..
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