Taiwan FDA registration a5ab2ebbace1791db902f73859887daa
“AERO” RapidStop Tourniquet (Non-sterile)
TW: “艾若” 銳霹速止血帶 (未滅菌)
Taiwan·Risk Class 1·MD·AERO HEALTHCARE US·Registered Jan 20, 2022 – Jan 20, 2027ActiveRegistration details
- Analysis ID
- a5ab2ebbace1791db902f73859887daa
- License Form
- Ministry of Health Medical Device Import No. 022732
- Customs Code
- DHA09402273200
Company information
- Manufacturer
- AERO HEALTHCARE US
- Manufacturer Country
- United States
- Authorized Representative
- CORELEADER BIOTECH 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)
- I5900 Non-inflatable tourniquet
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 20, 2022
- Expiry Date
- Jan 20, 2027
About this record
Access comprehensive regulatory information for “AERO” RapidStop Tourniquet (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5ab2ebbace1791db902f73859887daa and manufactured by AERO HEALTHCARE US. The authorized representative in Taiwan is CORELEADER BIOTECH CO., LTD..
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