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“B. Braun” Caresite Luer Access Device System - Taiwan Registration ca324a1b5e2d3f2a7859715dd8a9865d

Access comprehensive regulatory information for “B. Braun” Caresite Luer Access Device System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca324a1b5e2d3f2a7859715dd8a9865d and manufactured by B.BRAUN MEDICAL INC.. The authorized representative in Taiwan is B. BRAUN 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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ca324a1b5e2d3f2a7859715dd8a9865d
Registration Details
Taiwan FDA Registration: ca324a1b5e2d3f2a7859715dd8a9865d
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Device Details

“B. Braun” Caresite Luer Access Device System
TW: “柏朗”正可加延長導管組
Risk Class 2
MD

Registration Details

ca324a1b5e2d3f2a7859715dd8a9865d

Ministry of Health Medical Device Import No. 028554

DHA05602855409

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J5440 Intravascular infusion sleeve

Imported from abroad

Dates and Status

Apr 28, 2016

Apr 28, 2026