Taiwan FDA registration 8182fc4e30ab31d174e1a3ebfcba3829
NIPRO HEMODIAFILTER MAXIFLUX
TW: “尼普洛”血液透析器
Taiwan·Risk Class 2·MD·Nipro Corporation Odate Factory·Registered Jun 13, 2017 – Jun 13, 2027ActiveRegistration details
- Analysis ID
- 8182fc4e30ab31d174e1a3ebfcba3829
- License Form
- Ministry of Health Medical Device Import No. 029899
- Customs Code
- DHA05602989909
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
- Jun 13, 2017
- Expiry Date
- Jun 13, 2027
About this record
Access comprehensive regulatory information for NIPRO HEMODIAFILTER MAXIFLUX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8182fc4e30ab31d174e1a3ebfcba3829 and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
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