Taiwan FDA registration 36568f07d6289b6892cf61edfae24ca0
“Arthesys” Blizzard Balloon Catheters
TW: “亞提斯” 炫風冠狀動脈球囊導管
Taiwan·Risk Class 2·MD·ARTHESYS·Registered Aug 09, 2021 – Aug 09, 2026ActiveRegistration details
- Analysis ID
- 36568f07d6289b6892cf61edfae24ca0
- License Form
- Ministry of Health Medical Device Import No. 034780
- Customs Code
- DHA05603478004
Company information
- Manufacturer
- ARTHESYS
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 09, 2021
- Expiry Date
- Aug 09, 2026
About this record
Access comprehensive regulatory information for “Arthesys” Blizzard Balloon Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36568f07d6289b6892cf61edfae24ca0 and manufactured by ARTHESYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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