Taiwan FDA registration 6d7b1538c6377e61bb33399a56a4c595
"Keai Fusen" Miller Manual instruments for general surgery (unsterilized)
TW: “客愛福生” 米樂 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·CAREFUSION·Registered Sep 19, 2011 – Sep 19, 2021CancelledRegistration details
- Analysis ID
- 6d7b1538c6377e61bb33399a56a4c595
- Customs Code
- DHA04401085300
Company information
- Manufacturer
- CAREFUSION
- Manufacturer Country
- United States
- Authorized Representative
- CHAMPION MEDICAL CORPORATION
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
- Sep 19, 2011
- Expiry Date
- Sep 19, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Keai Fusen" Miller 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 6d7b1538c6377e61bb33399a56a4c595 and manufactured by CAREFUSION. The authorized representative in Taiwan is CHAMPION MEDICAL CORPORATION.
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