Taiwan FDA registration 15c44320834c9958ac5b0230da690ecb
"Zhaofeng" Weizhu polymer material cervical intervertebral fusion device
TW: “兆鋒”威拓高分子材料頸椎椎間融合器
Taiwan·Risk Class 2·TOPASIA INTERNATIONAL TECHNOLOGY INC.·Registered Sep 25, 2008 – Sep 25, 2013CancelledRegistration details
- Analysis ID
- 15c44320834c9958ac5b0230da690ecb
- Customs Code
- DHY00500250700
Company information
- Manufacturer
- TOPASIA INTERNATIONAL TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Zhaofeng Biotechnology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Sep 25, 2008
- Expiry Date
- Sep 25, 2013
- Cancellation Date
- Aug 10, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Zhaofeng" Weizhu polymer material cervical intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 15c44320834c9958ac5b0230da690ecb and manufactured by TOPASIA INTERNATIONAL TECHNOLOGY INC.. The authorized representative in Taiwan is Zhaofeng Biotechnology Co., Ltd.
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