Taiwan FDA registration 2fa89889426fce733d7e45783bafcd7c
"Guanya" hollow intervertebral fusion device
TW: “冠亞”中空椎間融合器
Taiwan·Risk Class 2·A-SPINE Asia Co., Ltd.·Registered Jun 26, 2007 – Jun 26, 2022CancelledRegistration details
- Analysis ID
- 2fa89889426fce733d7e45783bafcd7c
- Customs Code
- DHY00500222707
Company information
- Manufacturer
- A-SPINE Asia Co., Ltd.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A-SPINE Asia 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
- Domestic
Dates and status
- Registration Date
- Jun 26, 2007
- Expiry Date
- Jun 26, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業;;許可證已逾有效期;;未展延而逾期者
About this record
Access comprehensive regulatory information for "Guanya" hollow 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 2fa89889426fce733d7e45783bafcd7c and manufactured by A-SPINE Asia Co., Ltd.. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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