Vitrolife andrology system - Taiwan Registration 07b080f5d9a9f7ae0966016a6e61e50c
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..
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.
Device Details
Registration Details
07b080f5d9a9f7ae0966016a6e61e50c
Ministry of Health Medical Device Import No. 028604
DHA05602860401
Product Details
For details, it is Chinese approved copy of the imitation order
l Devices for obstetrics and gynecology
L6180 Reproductive vehicles and supplements
Imported from abroad
Dates and Status
Jun 13, 2016
Jun 13, 2026

