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Gilifol infusion tubing group - Taiwan Registration 0fd727bccf61c0869b2fc2496a4d6269

Access comprehensive regulatory information for Gilifol infusion tubing group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0fd727bccf61c0869b2fc2496a4d6269 and manufactured by Laboratorios Grifols, S.A.. The authorized representative in Taiwan is CONPLUS INTERNATIONAL 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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0fd727bccf61c0869b2fc2496a4d6269
Registration Details
Taiwan FDA Registration: 0fd727bccf61c0869b2fc2496a4d6269
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Device Details

Gilifol infusion tubing group
TW: ๅŸบ็ซ‹็ฆ่ผธๆถฒ็ฎก็ต„
Risk Class 2

Registration Details

0fd727bccf61c0869b2fc2496a4d6269

DHA00601958401

Company Information

Product Details

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

J General hospital and personal use equipment

J.5440 ่ก€็ฎกๅ…ง่ผธๆถฒๅฅ—

import

Dates and Status

Jan 23, 2009

Jan 23, 2029