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"Nipro" hollow fiber dialysis cylinder - Taiwan Registration 000d315a3663229fbe238c5619df4bcd

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 000d315a3663229fbe238c5619df4bcd 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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000d315a3663229fbe238c5619df4bcd
Registration Details
Taiwan FDA Registration: 000d315a3663229fbe238c5619df4bcd
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Device Details

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

Registration Details

000d315a3663229fbe238c5619df4bcd

DHA00602359801

Company Information

Product Details

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

H Gastroenterology and urology

H.5820 ่ก€ๆถฒ้€ๆž็ณป็ตฑๅŠๅ…ถ้™„ไปถ

import

Dates and Status

May 30, 2012

May 30, 2027

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