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Intravenous extension tubes - Taiwan Registration 21dc0da69866a285295b38122b51e0d9

Access comprehensive regulatory information for Intravenous extension tubes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21dc0da69866a285295b38122b51e0d9 and manufactured by BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including BOIN MEDICA CO., LTD., BAXTER HEALTHCARE CORPORATION, and 4 recent registrations in the same category. 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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21dc0da69866a285295b38122b51e0d9
Registration Details
Taiwan FDA Registration: 21dc0da69866a285295b38122b51e0d9
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Device Details

Intravenous extension tubes
TW: ้œๆณจๅปถ้•ท็ฎก
Risk Class 2
Cancelled

Registration Details

21dc0da69866a285295b38122b51e0d9

DHA00600862705

Company Information

United States

Product Details

Vacuum.

1305 Intravenous extension tube

import

Dates and Status

Apr 03, 1998

Oct 21, 2017

Nov 21, 2019

Cancellation Information

Logged out

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