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"Fresenius" synthetic membrane hemodialyzer - FX series - Taiwan Registration f196ef0db63ce4b1a4b5074c98bb0bd8

Access comprehensive regulatory information for "Fresenius" synthetic membrane hemodialyzer - FX series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f196ef0db63ce4b1a4b5074c98bb0bd8 and manufactured by FRESENIUS MEDICAL CARE SMAD. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FRESENIUS MEDICAL CARE JAPAN K.K. BUZEN PLANT, and 1 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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f196ef0db63ce4b1a4b5074c98bb0bd8
Registration Details
Taiwan FDA Registration: f196ef0db63ce4b1a4b5074c98bb0bd8
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Device Details

"Fresenius" synthetic membrane hemodialyzer - FX series
TW: โ€œ่ฒปๆฃฎๅฐคๆ–ฏโ€ไบบๅทฅๅˆๆˆ่†œ่ก€ๆถฒ้€ๆžๅ™จ- FX ็ณปๅˆ—
Risk Class 2

Registration Details

f196ef0db63ce4b1a4b5074c98bb0bd8

DHA00601833001

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

Sep 20, 2007

Sep 20, 2027

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