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"Nipro" hollow fiber dialysis cylinder - Taiwan Registration e9f352bea2a1017dfa16b7e396afcbfa

Access comprehensive regulatory information for "Nipro" hollow fiber dialysis cylinder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e9f352bea2a1017dfa16b7e396afcbfa and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including NIPRO CORPORATION ODATE FACTORY, Nipro Corporation Odate Factory, 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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e9f352bea2a1017dfa16b7e396afcbfa
Registration Details
Taiwan FDA Registration: e9f352bea2a1017dfa16b7e396afcbfa
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Device Details

"Nipro" hollow fiber dialysis cylinder
TW: "ๅฐผๆ™ฎๆด›"ไธญ็ฉบ็บ–็ถญ้€ๆž็ญ’
Risk Class 2
Cancelled

Registration Details

e9f352bea2a1017dfa16b7e396afcbfa

DHA00601056402

Company Information

Product Details

H Gastroenterology and urology

import

Dates and Status

Mar 02, 2004

Mar 02, 2019

Jun 07, 2022

Cancellation Information

Logged out

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