Taiwan FDA registration bf29cdf2576af398539a65ef5b58e53f
"Large medium" non-aerated tourniquet (unsterilized)
TW: "大中" 非充氣式止血帶 (未滅菌)
Taiwan·Risk Class 1·DA CHUNG MEDICAL CO., LTD.·Registered Nov 09, 2012 – Nov 09, 2017CancelledRegistration details
- Analysis ID
- bf29cdf2576af398539a65ef5b58e53f
Company information
- Manufacturer
- DA CHUNG MEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DA CHUNG MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5900 非充氣式止血帶
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 09, 2012
- Expiry Date
- Nov 09, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Large medium" non-aerated tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf29cdf2576af398539a65ef5b58e53f and manufactured by DA CHUNG MEDICAL CO., LTD.. The authorized representative in Taiwan is DA CHUNG MEDICAL CO., LTD..
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