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“Gambro” Prismaflex Set - Taiwan Registration 2f935a95d37d4ce47f5906386f38cf3f

Access comprehensive regulatory information for “Gambro” Prismaflex Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f935a95d37d4ce47f5906386f38cf3f and manufactured by GAMBRO INDUSTRIES. The authorized representative in Taiwan is BAXTER HEALTHCARE 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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2f935a95d37d4ce47f5906386f38cf3f
Registration Details
Taiwan FDA Registration: 2f935a95d37d4ce47f5906386f38cf3f
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Device Details

“Gambro” Prismaflex Set
TW: “衛寶”普利司連續性血液淨化套組
Risk Class 2
MD

Registration Details

2f935a95d37d4ce47f5906386f38cf3f

Ministry of Health Medical Device Import No. 025490

DHA05602549007

Company Information

France

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

Oct 08, 2013

Oct 08, 2023