NIPRO HEMODIAFILTER MAXIFLUX - Taiwan Registration 8182fc4e30ab31d174e1a3ebfcba3829
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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Device Details
Registration Details
8182fc4e30ab31d174e1a3ebfcba3829
Ministry of Health Medical Device Import No. 029899
DHA05602989909
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology-urology devices
H5860 Highly permeable hemodialysis system
Imported from abroad
Dates and Status
Jun 13, 2017
Jun 13, 2027