Taiwan FDA registration f5d2fd48a8388ec23035ac64bdd3ad0f
Vitrolife Follicle Aspiration Set
TW: 密陀來福取卵針
Taiwan·Risk Class 2·MD·Vitrolife Sweden AB·Registered May 18, 2015 – May 18, 2025ExpiredRegistration details
- Analysis ID
- f5d2fd48a8388ec23035ac64bdd3ad0f
- License Form
- Ministry of Health Medical Device Import No. 027295
- Customs Code
- DHA05602729506
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)
- L6100 Guide needle for assisted reproduction
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 18, 2015
- Expiry Date
- May 18, 2025
About this record
Access comprehensive regulatory information for Vitrolife Follicle Aspiration Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5d2fd48a8388ec23035ac64bdd3ad0f and manufactured by Vitrolife Sweden AB. The authorized representative in Taiwan is TSENG HSIANG LIFE SCIENCE LTD..
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