Taiwan FDA registration e30fa86e3e2c7b10008c637a4388fa9e
“NIKKISO” Hemodialysis Equipment
TW: “日機裝”人工腎臟裝置
Taiwan·Risk Class 2·MD·NIKKISO CO., LTD., KANAZAWA PLANT·Registered Dec 23, 2020 – Dec 23, 2025ExpiredRegistration details
- Analysis ID
- e30fa86e3e2c7b10008c637a4388fa9e
- License Form
- Ministry of Health Medical Device Import No. 034133
- Customs Code
- DHA05603413300
Company information
- Manufacturer
- NIKKISO CO., LTD., KANAZAWA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN NIKKISO CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5820 Hemodialysis systems and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 23, 2020
- Expiry Date
- Dec 23, 2025
About this record
Access comprehensive regulatory information for “NIKKISO” Hemodialysis Equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e30fa86e3e2c7b10008c637a4388fa9e and manufactured by NIKKISO CO., LTD., KANAZAWA PLANT. The authorized representative in Taiwan is TAIWAN NIKKISO CO., LTD..
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