Pure Global

"Kidme" germ cell culture reagent - Taiwan Registration 19d8d19132e38bf59844f9c196e23402

Access comprehensive regulatory information for "Kidme" germ cell culture reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19d8d19132e38bf59844f9c196e23402 and manufactured by GYNEMED GmbH & Co. KG. The authorized representative in Taiwan is MING-MEI TECHNOLOGY CO., 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
19d8d19132e38bf59844f9c196e23402
Registration Details
Taiwan FDA Registration: 19d8d19132e38bf59844f9c196e23402
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kidme" germ cell culture reagent
TW: โ€œๅ‰ๅพท็พŽโ€็”Ÿๆฎ–็ดฐ่ƒžๅŸน้คŠ่ฉฆๅŠ‘
Risk Class 2

Registration Details

19d8d19132e38bf59844f9c196e23402

DHA05603263307

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

l Obstetrics and Gynecology

L.6180 Vectors and supplements for reproductive use

import

Dates and Status

Jun 14, 2019

Jun 14, 2029