Taiwan FDA registration d22c47af06876eebc306a8c4be113719
"Guanya" spine surgery instruments (unsterilized)
TW: “冠亞” 脊椎手術器械 (未滅菌)
Taiwan·Risk Class 1·A-SPINE Asia Co., Ltd.·Registered Sep 11, 2009 – Sep 11, 2019CancelledRegistration details
- Analysis ID
- d22c47af06876eebc306a8c4be113719
- Customs Code
- DHY04300261701
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
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 11, 2009
- Expiry Date
- Sep 11, 2019
- 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" spine surgery instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d22c47af06876eebc306a8c4be113719 and manufactured by A-SPINE Asia Co., Ltd.. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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