Taiwan FDA registration 3110ecb9d1a456be520a640ef6881795
"Carneka" percutaneous cavaloplasty balloon catheter
TW: “卡內卡”經皮穿腔成型術氣球導管
Taiwan·Risk Class 2·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Apr 15, 2008 – Apr 15, 2023ExpiredRegistration details
- Analysis ID
- 3110ecb9d1a456be520a640ef6881795
- Customs Code
- DHA00601879901
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
- Apr 15, 2008
- Expiry Date
- Apr 15, 2023
About this record
Access comprehensive regulatory information for "Carneka" percutaneous cavaloplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3110ecb9d1a456be520a640ef6881795 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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