Taiwan FDA registration b48cbd0c02f2edc9ba7080eac41cf78d

Baxter Effluent Collection Bag (Sterilization)

TW: 〝百特〞濾出液收集袋 (滅菌)

Taiwan·Risk Class 1·Gambro UF Solutions, Inc.;; Made (部分製程) in DOMINICAN REPUBLIC·Registered Oct 08, 2019 – Oct 08, 2024Expired

Registration details

Analysis ID: b48cbd0c02f2edc9ba7080eac41cf78d
Customs Code: DHA09402093208

Company information

Manufacturer: Gambro UF Solutions, Inc.;; Made (部分製程) in DOMINICAN REPUBLIC
Manufacturer Country: Dominican Republic;;United States
Authorized Representative: BAXTER HEALTHCARE LTD.

Product details

Intended Use: 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.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.5820 血液透析系統及其附件
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Oct 08, 2019
Expiry Date: Oct 08, 2024

About this record

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..

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