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“Gynetics” Intrauterine Insemination Cannula - Taiwan Registration a87c3a2d24b75a2528bb2d3395300584

Access comprehensive regulatory information for “Gynetics” Intrauterine Insemination Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a87c3a2d24b75a2528bb2d3395300584 and manufactured by Gynetics Medical Products N.V.. 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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a87c3a2d24b75a2528bb2d3395300584
Registration Details
Taiwan FDA Registration: a87c3a2d24b75a2528bb2d3395300584
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Device Details

“Gynetics” Intrauterine Insemination Cannula
TW: “佳植”子宮內授精導管
Risk Class 2
MD

Registration Details

a87c3a2d24b75a2528bb2d3395300584

Ministry of Health Medical Device Import No. 025832

DHA05602583209

Company Information

Product Details

Intrauterine insemination catheters are mainly used for artificial insemination in utero.

l Devices for obstetrics and gynecology

L6110 Assisted reproductive catheter

Imported from abroad

Dates and Status

Mar 07, 2014

Mar 07, 2024