Taiwan FDA registration 4c1496d21a7a95a54efce28e8e45ce73
"Heiskei" Rika flick thrombus suction catheter
TW: “海斯凱” 芮卡拂血栓抽吸導管
Taiwan·Risk Class 2·Hexacath;; ARTHESYS·Registered Mar 02, 2021 – Mar 02, 2026ExpiredRegistration details
- Analysis ID
- 4c1496d21a7a95a54efce28e8e45ce73
- Customs Code
- DHA05603434703
Company information
- Manufacturer
- Hexacath;; ARTHESYS
- 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 Medicine Science
- Product Type (Level 2)
- E.5150 血栓切除術導管
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Mar 02, 2021
- Expiry Date
- Mar 02, 2026
About this record
Access comprehensive regulatory information for "Heiskei" Rika flick thrombus suction catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c1496d21a7a95a54efce28e8e45ce73 and manufactured by Hexacath;; ARTHESYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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