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"Nipro" Cardiopulmonary Vascular Bypass Assistive Device (Unsterilized) - Taiwan Registration 9b9b48cab0462ee0a9c1cc5022f13641

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..

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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9b9b48cab0462ee0a9c1cc5022f13641
Registration Details
Taiwan FDA Registration: 9b9b48cab0462ee0a9c1cc5022f13641
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Device Details

"Nipro" Cardiopulmonary Vascular Bypass Assistive Device (Unsterilized)
TW: "ๅฐผๆ™ฎๆด›" ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9b9b48cab0462ee0a9c1cc5022f13641

DHA09402102700

Company Information

Brazil

Product Details

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.

E Cardiovascular Medicine Science

E.4200 ๅฟƒ่‚บ่ก€็ฎก็นž้“่ก“่ผ”ๅŠฉ่จญๅ‚™

Input;; QMS/QSD

Dates and Status

Nov 20, 2019

Nov 20, 2029