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"Fresenius" synthetic membrane hemodialyzer - Taiwan Registration 04f0809103304fca69b834392ede7633

Access comprehensive regulatory information for "Fresenius" synthetic membrane hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 04f0809103304fca69b834392ede7633 and manufactured by FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including FRESENIUS MEDICAL CARE SMAD, FRESENIUS MEDICAL CARE JAPAN K.K. BUZEN PLANT, and 3 recent registrations in the same category. 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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04f0809103304fca69b834392ede7633
Registration Details
Taiwan FDA Registration: 04f0809103304fca69b834392ede7633
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Device Details

"Fresenius" synthetic membrane hemodialyzer
TW: "่ฒปๆฃฎๅฐคๆ–ฏ" ไบบๅทฅๅˆๆˆ่†œ่ก€ๆถฒ้€ๆžๅ™จ
Risk Class 2
Cancelled

Registration Details

04f0809103304fca69b834392ede7633

DHA00600982106

Company Information

Product Details

H Gastroenterology and urology

import

Dates and Status

Feb 01, 2002

Feb 01, 2017

Dec 20, 2019

Cancellation Information

Logged out

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