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"Haidi Liana" hollow fibrous hemodialyzer - Taiwan Registration 098c18b3a7bda96f1d31d4aa158c9e03

Access comprehensive regulatory information for "Haidi Liana" hollow fibrous hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 098c18b3a7bda96f1d31d4aa158c9e03 and manufactured by HAIDYLENA FOR ADVANCED MEDICAL INDUSTRIES. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..

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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098c18b3a7bda96f1d31d4aa158c9e03
Registration Details
Taiwan FDA Registration: 098c18b3a7bda96f1d31d4aa158c9e03
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Device Details

"Haidi Liana" hollow fibrous hemodialyzer
TW: "ๆตทๅธ้€ฃ็ด"ไธญ็ฉบ็บ–็ถญ่ก€ๆถฒ้€ๆžๅ™จ
Risk Class 2
Cancelled

Registration Details

098c18b3a7bda96f1d31d4aa158c9e03

DHA00601764600

Company Information

Product Details

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

H Gastroenterology and urology

H.5860 ้ซ˜ๆปฒ้€ๆ€งไน‹่ก€ๆถฒ้€ๆž็ณป็ตฑ

import

Dates and Status

Dec 29, 2006

Dec 29, 2016

Apr 25, 2018

Cancellation Information

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