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Baxter Effluent Collection Bag (Sterilization) - Taiwan Registration b48cbd0c02f2edc9ba7080eac41cf78d

Access comprehensive regulatory information for Baxter Effluent Collection Bag (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b48cbd0c02f2edc9ba7080eac41cf78d and manufactured by Gambro UF Solutions, Inc.;; Made (部分製程) in DOMINICAN REPUBLIC. 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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b48cbd0c02f2edc9ba7080eac41cf78d
Registration Details
Taiwan FDA Registration: b48cbd0c02f2edc9ba7080eac41cf78d
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Device Details

Baxter Effluent Collection Bag (Sterilization)
TW: 〝百特〞濾出液收集袋 (滅菌)
Risk Class 1

Registration Details

b48cbd0c02f2edc9ba7080eac41cf78d

DHA09402093208

Company Information

Product Details

It is limited to the scope of the first level of identification of the "Hemodialysis System and Its Accessories (H.5820)" of the Measures for the Classification and Grading of Medical Devices.

H Gastroenterology and urology

H.5820 血液透析系統及其附件

Input;; QMS/QSD

Dates and Status

Oct 08, 2019

Oct 08, 2024