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"Braun" Vivida infusion tube group - Taiwan Registration 55bf589c44d63cc9d85fb75dd4d07fb0

Access comprehensive regulatory information for "Braun" Vivida infusion tube group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55bf589c44d63cc9d85fb75dd4d07fb0 and manufactured by B.BRAUN MELSUNGEN AG. The authorized representative in Taiwan is NOVARTIS (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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55bf589c44d63cc9d85fb75dd4d07fb0
Registration Details
Taiwan FDA Registration: 55bf589c44d63cc9d85fb75dd4d07fb0
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Device Details

"Braun" Vivida infusion tube group
TW: "ๆŸๆœ—" ็ถญ่ฆ–้”่ผธๆณจ็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

55bf589c44d63cc9d85fb75dd4d07fb0

DHA00601037002

Company Information

Germany

Product Details

J General hospital and personal use equipment

import

Dates and Status

Aug 19, 2003

Aug 19, 2018

Aug 05, 2022

Cancellation Information

Logged out

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