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"Japanese machine-mounted" hollow fibrous hemodialysis tube - Taiwan Registration 3e5bd4c216f1ea1b7429af912694c287

Access comprehensive regulatory information for "Japanese machine-mounted" hollow fibrous hemodialysis tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e5bd4c216f1ea1b7429af912694c287 and manufactured by NIKKISO CO., LTD., KANAZAWA PLANT. The authorized representative in Taiwan is TAIWAN NIKKISO 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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3e5bd4c216f1ea1b7429af912694c287
Registration Details
Taiwan FDA Registration: 3e5bd4c216f1ea1b7429af912694c287
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Device Details

"Japanese machine-mounted" hollow fibrous hemodialysis tube
TW: "ๆ—ฅๆฉŸ่ฃ" ไธญ็ฉบ็บ–็ถญๅž‹่ก€ๆถฒ้€ๆž็ญ’
Risk Class 2
Cancelled

Registration Details

3e5bd4c216f1ea1b7429af912694c287

DHA00601046306

Company Information

Product Details

H Gastroenterology and urology

import

Dates and Status

Nov 13, 2003

Nov 13, 2018

Jul 15, 2022

Cancellation Information

Logged out

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