Taiwan FDA registration 7d7929ac55e878623a6be50631a949f7
“Dynamesh” Mesh implants for female urinary incontinence
TW: “黛娜美”女性尿失禁手術用網片
Taiwan·Risk Class 2·MD·FEG Textiltechnik, Forschungs-und Entwicklungsgesellschaft mbH·Registered Sep 26, 2017 – Sep 26, 2027ActiveRegistration details
- Analysis ID
- 7d7929ac55e878623a6be50631a949f7
- License Form
- Ministry of Health Medical Device Import No. 030301
- Customs Code
- DHA05603030101
Company information
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3300 Surgical mesh
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 26, 2017
- Expiry Date
- Sep 26, 2027
About this record
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.
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