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“Dynamesh” Mesh implants for female urinary incontinence - Taiwan Registration 7d7929ac55e878623a6be50631a949f7

Access comprehensive regulatory information for “Dynamesh” Mesh implants for female urinary incontinence in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d7929ac55e878623a6be50631a949f7 and manufactured by FEG Textiltechnik, Forschungs-und Entwicklungsgesellschaft mbH. The authorized representative in Taiwan is Huizhong 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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7d7929ac55e878623a6be50631a949f7
Registration Details
Taiwan FDA Registration: 7d7929ac55e878623a6be50631a949f7
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Device Details

“Dynamesh” Mesh implants for female urinary incontinence
TW: “黛娜美”女性尿失禁手術用網片
Risk Class 2
MD

Registration Details

7d7929ac55e878623a6be50631a949f7

Ministry of Health Medical Device Import No. 030301

DHA05603030101

Company Information

Product Details

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

I General and plastic surgical devices

I3300 Surgical mesh

Imported from abroad

Dates and Status

Sep 26, 2017

Sep 26, 2027