Taiwan FDA registration 21271300c75cc9a6f50a341b107c3761
"Guanya" spine manual surgical instruments (sterilization)
TW: “冠亞”脊椎手動式手術用器械 (滅菌)
Taiwan·Risk Class 1·TOPASIA INTERNATIONAL TECHNOLOGY INC.·Registered Sep 05, 2007 – Sep 05, 2012CancelledRegistration details
- Analysis ID
- 21271300c75cc9a6f50a341b107c3761
Company information
- Manufacturer
- TOPASIA INTERNATIONAL TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TOPASIA INTERNATIONAL TECHNOLOGY INC.
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
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Sep 05, 2007
- Expiry Date
- Sep 05, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Guanya" spine manual surgical instruments (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 21271300c75cc9a6f50a341b107c3761 and manufactured by TOPASIA INTERNATIONAL TECHNOLOGY INC.. The authorized representative in Taiwan is TOPASIA INTERNATIONAL TECHNOLOGY INC..
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