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“Dynamesh” Mesh for Female Pelvic Floor Surgery - Taiwan Registration 61b9898b8fa06e67d9b8e1a41a2bb23d

Access comprehensive regulatory information for “Dynamesh” Mesh for Female Pelvic Floor Surgery in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61b9898b8fa06e67d9b8e1a41a2bb23d 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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61b9898b8fa06e67d9b8e1a41a2bb23d
Registration Details
Taiwan FDA Registration: 61b9898b8fa06e67d9b8e1a41a2bb23d
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Device Details

“Dynamesh” Mesh for Female Pelvic Floor Surgery
TW: “黛娜美”女性骨盆底修復網片
Risk Class 2
MD

Registration Details

61b9898b8fa06e67d9b8e1a41a2bb23d

Ministry of Health Medical Device Import No. 030302

DHA05603030200

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 28, 2017

Sep 28, 2027