Taiwan FDA registration 1910c6884d20efd2978ff2ee23049b74
“Nipro” Hemodiafilter Fineflux
TW: “尼普洛”血液透析器
Taiwan·Risk Class 2·MD·Nipro Corporation Odate Factory·Registered Nov 01, 2016 – Nov 01, 2026ActiveRegistration details
- Analysis ID
- 1910c6884d20efd2978ff2ee23049b74
- License Form
- Ministry of Health Medical Device Import No. 029009
- Customs Code
- DHA05602900902
Company information
- Manufacturer
- Nipro Corporation Odate Factory
- Manufacturer Country
- Japan
- Authorized Representative
- HUA CHIANG MEDICAL 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)
- H5860 Highly permeable hemodialysis system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 01, 2016
- Expiry Date
- Nov 01, 2026
About this record
Access comprehensive regulatory information for “Nipro” Hemodiafilter Fineflux in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1910c6884d20efd2978ff2ee23049b74 and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
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