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“AMS” LiquiBand Hernia Mesh Fixation Device - Taiwan Registration 716ec1921d178c3fb958f07ff5b0af08

Access comprehensive regulatory information for “AMS” LiquiBand Hernia Mesh Fixation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 716ec1921d178c3fb958f07ff5b0af08 and manufactured by Advanced Medical Solutions Limited. The authorized representative in Taiwan is MEDLION BIOTECH 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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716ec1921d178c3fb958f07ff5b0af08
Registration Details
Taiwan FDA Registration: 716ec1921d178c3fb958f07ff5b0af08
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Device Details

“AMS” LiquiBand Hernia Mesh Fixation Device
TW: “艾曼斯”立可棒疝氣修補網片黏著劑
Risk Class 3
MD

Registration Details

716ec1921d178c3fb958f07ff5b0af08

Ministry of Health Medical Device Import No. 030122

DHA05603012201

Company Information

United Kingdom

Product Details

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

I General and plastic surgical devices

I4010 Tissue adhesives

Imported from abroad

Dates and Status

Aug 18, 2017

Aug 18, 2027