Taiwan FDA registration 7835e1f346ebdcecbe5ce8db2a862878
"Apo" IVF micromanipulation tube
TW: “亞樸” 體外受精顯微操作管
Taiwan·Risk Class 2·Vitrolife Sweden AB·Registered Aug 07, 2024 – Aug 07, 2029ActiveRegistration details
- Analysis ID
- 7835e1f346ebdcecbe5ce8db2a862878
- Customs Code
- DHA05603727302
Company information
- Manufacturer
- Vitrolife Sweden AB
- Manufacturer Country
- Sweden
- Authorized Representative
- unitedparadise technology Limited
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.6130 輔助生殖之微小器具
- Import Information
- import
Dates and status
- Registration Date
- Aug 07, 2024
- Expiry Date
- Aug 07, 2029
About this record
Access comprehensive regulatory information for "Apo" IVF micromanipulation tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7835e1f346ebdcecbe5ce8db2a862878 and manufactured by Vitrolife Sweden AB. The authorized representative in Taiwan is unitedparadise technology Limited.
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.
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