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“Cavex” Quadrant Flow Composite - Taiwan Registration a9131a1a37849e4c505e41dd8fd51a4f

Access comprehensive regulatory information for “Cavex” Quadrant Flow Composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9131a1a37849e4c505e41dd8fd51a4f and manufactured by CAVEX HOLLAND B.V.. The authorized representative in Taiwan is MONITEX INDUSTRIAL 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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a9131a1a37849e4c505e41dd8fd51a4f
Registration Details
Taiwan FDA Registration: a9131a1a37849e4c505e41dd8fd51a4f
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Device Details

“Cavex” Quadrant Flow Composite
TW: “佳貝士”夸任特流動性複合材
Risk Class 2
MD

Registration Details

a9131a1a37849e4c505e41dd8fd51a4f

Ministry of Health Medical Device Import No. 028187

DHA05602818708

Company Information

Netherlands

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Feb 03, 2016

Feb 03, 2026