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“Fresenius” MultiFiltrate Pro System - Taiwan Registration 78811c7d677bbaac8462d8d3c5912c1c

Access comprehensive regulatory information for “Fresenius” MultiFiltrate Pro System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78811c7d677bbaac8462d8d3c5912c1c and manufactured by Fresenius Medical Care Deutschland GmbH Schweinfurt Plant. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN 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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78811c7d677bbaac8462d8d3c5912c1c
Registration Details
Taiwan FDA Registration: 78811c7d677bbaac8462d8d3c5912c1c
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Device Details

“Fresenius” MultiFiltrate Pro System
TW: “費森尤斯” 多重過濾普羅系統
Risk Class 2
MD

Registration Details

78811c7d677bbaac8462d8d3c5912c1c

Ministry of Health Medical Device Import No. 028460

DHA05602846000

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

Jul 22, 2016

Jul 22, 2026