Taiwan FDA registration dd77ebbafb91043719c580a447c82a02
"Ampra" manual instruments for general surgery (unsterilized)
TW: “安普拉”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·APOLLO SURGICAL INDUSTRIES, INC.·Registered Jan 03, 2012 – Jan 03, 2017CancelledRegistration details
- Analysis ID
- dd77ebbafb91043719c580a447c82a02
- Customs Code
- DHA04401126208
Company information
- Manufacturer
- APOLLO SURGICAL INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ANGEL MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Jan 03, 2012
- Expiry Date
- Jan 03, 2017
- Cancellation Date
- Nov 18, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ampra" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd77ebbafb91043719c580a447c82a02 and manufactured by APOLLO SURGICAL INDUSTRIES, INC.. The authorized representative in Taiwan is ANGEL MEDICAL INSTRUMENT CO., LTD..
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