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“Vitrolife” culture system - Taiwan Registration b6b059bb8542882c9226d8f84ba18433

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..

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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b6b059bb8542882c9226d8f84ba18433
Registration Details
Taiwan FDA Registration: b6b059bb8542882c9226d8f84ba18433
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Device Details

“Vitrolife” culture system
TW: “密陀來福”生殖細胞培養系統
Risk Class 2
MD

Registration Details

b6b059bb8542882c9226d8f84ba18433

Ministry of Health Medical Device Import No. 028132

DHA05602813209

Company Information

Sweden

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

Jan 05, 2016

Jan 05, 2026