Taiwan FDA registration 61b9898b8fa06e67d9b8e1a41a2bb23d
“Dynamesh” Mesh for Female Pelvic Floor Surgery
TW: “黛娜美”女性骨盆底修復網片
Taiwan·Risk Class 2·MD·FEG Textiltechnik, Forschungs-und Entwicklungsgesellschaft mbH·Registered Sep 28, 2017 – Sep 28, 2027ActiveRegistration details
- Analysis ID
- 61b9898b8fa06e67d9b8e1a41a2bb23d
- License Form
- Ministry of Health Medical Device Import No. 030302
- Customs Code
- DHA05603030200
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 28, 2017
- Expiry Date
- Sep 28, 2027
About this record
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.
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