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〝Nidacon〞PureSperm - Taiwan Registration d1ba2a1f7e24dcff351cee237df1ebb9

Access comprehensive regulatory information for 〝Nidacon〞PureSperm in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d1ba2a1f7e24dcff351cee237df1ebb9 and manufactured by NIDACON INTERNATIONAL AB. 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.

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d1ba2a1f7e24dcff351cee237df1ebb9
Registration Details
Taiwan FDA Registration: d1ba2a1f7e24dcff351cee237df1ebb9
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Device Details

〝Nidacon〞PureSperm
TW: 〝尼達生〞男性不孕症試劑
Risk Class 2
MD

Registration Details

d1ba2a1f7e24dcff351cee237df1ebb9

Ministry of Health Medical Device Import No. 035518

DHA05603551809

Company Information

Sweden

Product Details

Details are as detailed as approved Chinese instructions

l Obstetrics and Gynecology

L6180 Reproductive vehicles and supplements

Imported from abroad

Dates and Status

Jul 03, 2022

Jul 03, 2027