Taiwan FDA registration 793241a8532940dea2cf45da6b35d18d
"Carneka" coronary angioplasty probes the catheter
TW: "卡內卡"冠狀動脈成型術探測導管
Taiwan·Risk Class 2·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Oct 23, 2006 – Oct 23, 2026ActiveRegistration details
- Analysis ID
- 793241a8532940dea2cf45da6b35d18d
- Customs Code
- DHA00601736706
Company information
- Manufacturer
- KANEKA MEDIX CORPORATION KANAGAWA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2006
- Expiry Date
- Oct 23, 2026
About this record
Access comprehensive regulatory information for "Carneka" coronary angioplasty probes the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 793241a8532940dea2cf45da6b35d18d and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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