Taiwan FDA registration 913d0ff51deddfec0b3ed5f5fcf4fbff
Ankmerx Bone Fixation Bone Nail Series
TW: 安克美骨內固定骨釘系列
Taiwan·Risk Class 2·Weigang Biotechnology Co., Ltd. Triple Second Factory·Registered Jan 18, 2007 – Jan 18, 2017CancelledRegistration details
- Analysis ID
- 913d0ff51deddfec0b3ed5f5fcf4fbff
- Customs Code
- DHY00500212308
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Weigang Biotechnology Co., Ltd. triple plant
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4880 骨內固定螺釘或金屬線
Dates and status
- Registration Date
- Jan 18, 2007
- Expiry Date
- Jan 18, 2017
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ankmerx Bone Fixation Bone Nail Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 913d0ff51deddfec0b3ed5f5fcf4fbff and manufactured by Weigang Biotechnology Co., Ltd. Triple Second Factory. The authorized representative in Taiwan is Weigang Biotechnology Co., Ltd. triple plant.
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