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"Fresenius" and the membrane flow artificial kidney - Taiwan Registration 0d96c622ac928b2d4bc85b4e9c5528af

Access comprehensive regulatory information for "Fresenius" and the membrane flow artificial kidney in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d96c622ac928b2d4bc85b4e9c5528af and manufactured by FRESENIUS MEDICAL CARE NORTH AMERICA. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN 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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0d96c622ac928b2d4bc85b4e9c5528af
Registration Details
Taiwan FDA Registration: 0d96c622ac928b2d4bc85b4e9c5528af
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Device Details

"Fresenius" and the membrane flow artificial kidney
TW: โ€œ่ฒปๆฃฎๅฐคๆ–ฏโ€ๅ’Œ่†œๆตไบบๅทฅ่…Ž่‡Ÿ
Risk Class 2

Registration Details

0d96c622ac928b2d4bc85b4e9c5528af

DHA00602072901

Company Information

United States

Product Details

Fresenius and Membrane Flow Series artificial kidneys are designed for acute and chronic hemodialysis and are suitable for single and multiple use. When going through the reprocessing process, please follow the method described or recommended in this product manual. Multiple uses by the same patient only.

H Gastroenterology and urology

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

import

Dates and Status

Nov 26, 2009

Nov 26, 2024