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"Apo" germ cell culture system - Taiwan Registration 030975eaf074543beee2109f8c522a02

Access comprehensive regulatory information for "Apo" germ cell 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 030975eaf074543beee2109f8c522a02 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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030975eaf074543beee2109f8c522a02
Registration Details
Taiwan FDA Registration: 030975eaf074543beee2109f8c522a02
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Device Details

"Apo" germ cell culture system
TW: โ€œไบžๆจธโ€ ็”Ÿๆฎ–็ดฐ่ƒžๅŸน้คŠ็ณป็ตฑ
Risk Class 2

Registration Details

030975eaf074543beee2109f8c522a02

DHA05603729907

Company Information

Sweden

Product Details

Details are as detailed as approved Chinese instructions

l Obstetrics and Gynecology

L.6180 Vectors and supplements for reproductive use

import

Dates and Status

Sep 06, 2024

Sep 06, 2029