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"Aixiyo" Digo hemodialysis connector - Taiwan Registration d6672752efa6f5d6e51e603f4fb98024

Access comprehensive regulatory information for "Aixiyo" Digo hemodialysis connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d6672752efa6f5d6e51e603f4fb98024 and manufactured by ICU MEDICAL, INC.. The authorized representative in Taiwan is EVERMEDICAL COMPANY 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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d6672752efa6f5d6e51e603f4fb98024
Registration Details
Taiwan FDA Registration: d6672752efa6f5d6e51e603f4fb98024
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Device Details

"Aixiyo" Digo hemodialysis connector
TW: โ€œๆ„›่ฅฟๅ„ชโ€่ฟช้ซ˜่ก€ๆถฒ้€ๆžๆŽฅ้ ญ
Risk Class 2
Cancelled

Registration Details

d6672752efa6f5d6e51e603f4fb98024

DHA00602443106

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

import

Dates and Status

Jan 10, 2013

Jan 10, 2018

Dec 20, 2019

Cancellation Information

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