Taiwan FDA registration a6f080241c73b84c1501f2941f45a837
“Kaneka” i-ED COIL System
TW: “卡內卡”可脫離線圈系統
Taiwan·Risk Class 3·MD·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered May 17, 2022 – May 17, 2027ActiveRegistration details
- Analysis ID
- a6f080241c73b84c1501f2941f45a837
- License Form
- Ministry of Health Medical Device Import No. 035475
- Customs Code
- DHA05603547504
Company information
- Manufacturer
- KANEKA MEDIX CORPORATION KANAGAWA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K5950 Artificial embolization device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 17, 2022
- Expiry Date
- May 17, 2027
About this record
Access comprehensive regulatory information for “Kaneka” i-ED COIL System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a6f080241c73b84c1501f2941f45a837 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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