Taiwan FDA registration d4a5c1962f510bcc4ffef7b9b3312791
"Guanya" hynix lumbar intervertebral fusion device
TW: "冠亞" 海力士腰椎椎間融合器
Taiwan·Risk Class 2·A-SPINE Asia Co., Ltd.·Registered May 03, 2005 – May 03, 2020CancelledRegistration details
- Analysis ID
- d4a5c1962f510bcc4ffef7b9b3312791
- Customs Code
- DHY00500133709
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
- Import Information
- Domestic
Dates and status
- Registration Date
- May 03, 2005
- Expiry Date
- May 03, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Guanya" hynix 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 d4a5c1962f510bcc4ffef7b9b3312791 and manufactured by A-SPINE Asia Co., Ltd.. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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