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"Baxter" Effluent Collection Bag (Sterilization) - Taiwan Registration 4c6475453a71a497385b1193e6757b0d

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 4c6475453a71a497385b1193e6757b0d and manufactured by GAMBRO DASCO S.p.A.; Made (部分製程) in SLOVENIA. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Baxter Limited;; GAMBRO DASCO S.p.A., and 1 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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4c6475453a71a497385b1193e6757b0d
Registration Details
Taiwan FDA Registration: 4c6475453a71a497385b1193e6757b0d
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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

4c6475453a71a497385b1193e6757b0d

DHA09402101707

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

QMS/QSD;; 輸入

Dates and Status

Nov 15, 2019

Nov 15, 2029

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