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"PulseCath" iVAC 2L Percutaneous Ventricular Assist Device - Taiwan Registration fd9b28423cf398764bbed4c1b8b3b680

Access comprehensive regulatory information for "PulseCath" iVAC 2L Percutaneous Ventricular Assist Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fd9b28423cf398764bbed4c1b8b3b680 and manufactured by PulseCath B.V.. The authorized representative in Taiwan is WIN CHAMP 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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fd9b28423cf398764bbed4c1b8b3b680
Registration Details
Taiwan FDA Registration: fd9b28423cf398764bbed4c1b8b3b680
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Device Details

"PulseCath" iVAC 2L Percutaneous Ventricular Assist Device
TW: "ๅšๆ–ฏๅ‡ฑ" ๆ„›้Ÿ‹ๅ…‹็ถ“็šฎๅผๅฟƒๅฎค่ผ”ๅŠฉ่ฃ็ฝฎ
Risk Class 3
MD

Registration Details

fd9b28423cf398764bbed4c1b8b3b680

Ministry of Health Medical Device Import No. 035968

DHA05603596801

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E9999 Other

Imported from abroad

Dates and Status

Oct 21, 2022

Oct 21, 2027