Taiwan FDA registration 242f8ec28eb652bb7cc43d76f168240c
KANEKA Micro Catheter
TW: “卡內卡”微導管
Taiwan·Risk Class 2·MD·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Dec 07, 2019 – Dec 07, 2024ExpiredRegistration details
- Analysis ID
- 242f8ec28eb652bb7cc43d76f168240c
- License Form
- Ministry of Health Medical Device Import No. 033059
- Customs Code
- DHA05603305906
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 devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 07, 2019
- Expiry Date
- Dec 07, 2024
About this record
Access comprehensive regulatory information for KANEKA Micro Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 242f8ec28eb652bb7cc43d76f168240c and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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