Taiwan FDA registration 7c93730255a0aeeeabadd78eab8194c8
"Aconn" Catheter Fixation Device (Sterilized)
TW: “亞康恩” 導管固定裝置 (滅菌)
Taiwan·Risk Class 1·ARGON MEDICAL DEVICES, INC.·Registered Sep 21, 2023 – Sep 21, 2028ActiveRegistration details
- Analysis ID
- 7c93730255a0aeeeabadd78eab8194c8
- Customs Code
- DHA09402325000
Company information
- Manufacturer
- ARGON MEDICAL DEVICES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the classification and grading management method of medical equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5210 血管內導管固定裝置
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 21, 2023
- Expiry Date
- Sep 21, 2028
About this record
Access comprehensive regulatory information for "Aconn" Catheter Fixation Device (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7c93730255a0aeeeabadd78eab8194c8 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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