Vitrolife Micromanipulation Pipettes - Taiwan Registration 925fb5941647f4ba4ac0bd2ee85c88ca
Access comprehensive regulatory information for Vitrolife Micromanipulation Pipettes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 925fb5941647f4ba4ac0bd2ee85c88ca 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, 1 companies making similar products including Vitrolife Inc., and 1 recent registrations in the same category. 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
925fb5941647f4ba4ac0bd2ee85c88ca
Ministry of Health Medical Device Import No. 027304
DHA05602730407
Product Details
For details, it is Chinese approved copy of the imitation order
l Devices for obstetrics and gynecology
L6130 Tiny apparatus for assisted reproduction
Imported from abroad
Dates and Status
May 26, 2015
May 26, 2025

