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“Nipro” Hemodialyzer - Taiwan Registration 12a52f7002c154f6e8fbeb748f1d6bfb

Access comprehensive regulatory information for “Nipro” Hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12a52f7002c154f6e8fbeb748f1d6bfb and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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12a52f7002c154f6e8fbeb748f1d6bfb
Registration Details
Taiwan FDA Registration: 12a52f7002c154f6e8fbeb748f1d6bfb
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Device Details

“Nipro” Hemodialyzer
TW: “尼普洛”中空纖維透析筒
Risk Class 2
MD

Registration Details

12a52f7002c154f6e8fbeb748f1d6bfb

Ministry of Health Medical Device Import No. 031932

DHA05603193202

Company Information

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

Dec 20, 2018

Dec 20, 2028