Taiwan FDA registration 8226bd3bc82e0a997fe1e4d1fe8f038f
"Heskei" cyclone coronary balloon dilation catheter
TW: “海斯凱”旋風冠狀動脈氣球擴張導管
Taiwan·Risk Class 3·HEXACATH·Registered Dec 17, 2007 – Dec 17, 2017CancelledRegistration details
- Analysis ID
- 8226bd3bc82e0a997fe1e4d1fe8f038f
- Customs Code
- DHA00601850408
Company information
- Manufacturer
- HEXACATH
- Manufacturer Country
- France
- Authorized Representative
- WATTCAN INSTRUMENTS 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.0005.
- Import Information
- import
Dates and status
- Registration Date
- Dec 17, 2007
- Expiry Date
- Dec 17, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heskei" cyclone coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8226bd3bc82e0a997fe1e4d1fe8f038f and manufactured by HEXACATH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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