Taiwan FDA registration 1d04d72f0eeb636d3604b70831b8edb2
"Carneca" Ryan bile duct dilation balloon catheter
TW: “卡內卡”瑞恩膽管擴張氣球導管
Taiwan·Risk Class 2·KANEKA CORPORATION;; KANEKA CORPORATION OSAKA PLANT·Registered Aug 21, 2023 – Aug 21, 2028ActiveRegistration details
- Analysis ID
- 1d04d72f0eeb636d3604b70831b8edb2
- Customs Code
- DHA05603669905
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5010 膽管用導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2023
- Expiry Date
- Aug 21, 2028
About this record
Access comprehensive regulatory information for "Carneca" Ryan bile duct dilation 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 1d04d72f0eeb636d3604b70831b8edb2 and manufactured by KANEKA CORPORATION;; KANEKA CORPORATION OSAKA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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