Taiwan FDA registration 34526e6059a0c78fa173a7fe19f056e8
“Argon” Vessel Dilators
TW: “亞康恩”血管擴張器
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Jan 18, 2019 – Jan 18, 2029ActiveRegistration details
- Analysis ID
- 34526e6059a0c78fa173a7fe19f056e8
- License Form
- Ministry of Health Medical Device Import No. 032079
- Customs Code
- DHA05603207907
Company information
- Manufacturer
- ARGON MEDICAL DEVICES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1310 Vasodilator for percutaneous catheters
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 18, 2019
- Expiry Date
- Jan 18, 2029
About this record
Access comprehensive regulatory information for “Argon” Vessel Dilators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 34526e6059a0c78fa173a7fe19f056e8 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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