Taiwan FDA registration 6128e60435fbb4c53b131a2b4279ca2e
"Shanglun" non-aerated tourniquet (unsterilized)
TW: “尚倫”非充氣式止血帶 (未滅菌)
Taiwan·Risk Class 1·HONG AN MEDICAL APPLIANCE CO., LTD.·Registered Jul 30, 2008 – Jul 30, 2028ActiveRegistration details
- Analysis ID
- 6128e60435fbb4c53b131a2b4279ca2e
- Customs Code
- DHA04600055209
Company information
- Manufacturer
- HONG AN MEDICAL APPLIANCE CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- SHAN-LUEN MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "non-inflatable tourniquet (I.5900)" of the Measures for the Classification and Grading of Medical Devices.
- 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 30, 2008
- Expiry Date
- Jul 30, 2028
About this record
Access comprehensive regulatory information for "Shanglun" 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 6128e60435fbb4c53b131a2b4279ca2e and manufactured by HONG AN MEDICAL APPLIANCE CO., LTD.. The authorized representative in Taiwan is SHAN-LUEN MEDICAL CO., LTD..
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