"Zhaofeng" Weizhou polymer material lumbar intervertebral fusion device
Taiwan·Risk Class 2·Zhaofeng Biotech Co., Ltd.;; Guanya International Technology Co., Ltd·Registered Sep 25, 2008 – Sep 25, 2013Cancelled- Analysis ID
- 3c213ed19a0041008d99a00be24f2536
- Customs Code
- DHY00500250802
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Zhaofeng Biotechnology Co., Ltd
- 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
- Domestic
- Registration Date
- Sep 25, 2008
- Expiry Date
- Sep 25, 2013
- Cancellation Date
- Aug 10, 2015
- Status
- Logged out
- Reason
- 許可證已逾有效期
Access comprehensive regulatory information for "Zhaofeng" Weizhou polymer material lumbar 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 3c213ed19a0041008d99a00be24f2536 and manufactured by Zhaofeng Biotech Co., Ltd.;; Guanya International Technology Co., Ltd. The authorized representative in Taiwan is Zhaofeng Biotechnology Co., Ltd.
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