Vitrolife Micromanipulation Pipettes - Taiwan Registration 0991124e20be6c98869187195a4efe7c
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 0991124e20be6c98869187195a4efe7c and manufactured by Vitrolife Inc.. 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 Sweden AB, 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
0991124e20be6c98869187195a4efe7c
Ministry of Health Medical Device Import No. 027027
DHA05602702707
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
Feb 26, 2015
Feb 26, 2025

