Taiwan FDA registration 9b9b48cab0462ee0a9c1cc5022f13641

"Nipro" Cardiopulmonary Vascular Bypass Assistive Device (Unsterilized)

TW: "尼普洛" 心肺血管繞道術輔助設備 (未滅菌)

Taiwan·Risk Class 1·Nipro Medical Ltda.·Registered Nov 20, 2019 – Nov 20, 2029Active

Registration details

Analysis ID: 9b9b48cab0462ee0a9c1cc5022f13641
Customs Code: DHA09402102700

Company information

Manufacturer: Nipro Medical Ltda.
Manufacturer Country: Brazil
Authorized Representative: HUA CHIANG MEDICAL CO., LTD.

Product details

Intended Use: It is limited to the first level identification scope of cardiopulmonary vascular bypass auxiliary equipment (E.4200) of the classification and grading management measures for medical devices.
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.4200 心肺血管繞道術輔助設備
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Nov 20, 2019
Expiry Date: Nov 20, 2029

About this record

Access comprehensive regulatory information for "Nipro" Cardiopulmonary Vascular Bypass Assistive Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b9b48cab0462ee0a9c1cc5022f13641 and manufactured by Nipro Medical Ltda.. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..

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