Taiwan FDA registration 43390b0fb53cd95db90f5c9e22a19f64
“HEXACATH” RayFlow Multipurpose Infusion Catheter
TW: “海斯凱”瑞菲多功能灌注導管
Taiwan·Risk Class 2·MD·HEXACATH·Registered Jul 07, 2020 – Jul 07, 2025ExpiredRegistration details
- Analysis ID
- 43390b0fb53cd95db90f5c9e22a19f64
- License Form
- Ministry of Health Medical Device Import No. 033808
- Customs Code
- DHA05603380808
Company information
- Manufacturer
- HEXACATH
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS 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)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 07, 2020
- Expiry Date
- Jul 07, 2025
About this record
Access comprehensive regulatory information for “HEXACATH” RayFlow Multipurpose Infusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43390b0fb53cd95db90f5c9e22a19f64 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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