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“MediFirst” CATH PRO I.V Catheter - Taiwan Registration 0631c9234659ea29e2264e32a88aa600

Access comprehensive regulatory information for “MediFirst” CATH PRO I.V Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0631c9234659ea29e2264e32a88aa600 and manufactured by MediFirst Co., Ltd.. The authorized representative in Taiwan is GREAT KUEI TAI INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MediFirst Co., Ltd., 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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0631c9234659ea29e2264e32a88aa600
Registration Details
Taiwan FDA Registration: 0631c9234659ea29e2264e32a88aa600
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Device Details

“MediFirst” CATH PRO I.V Catheter
TW: “美德芙”靜脈留置針
Risk Class 2
MD
Cancelled

Registration Details

0631c9234659ea29e2264e32a88aa600

Ministry of Health Medical Device Import No. 025384

DHA05602538408

Company Information

Korea, Republic of

Product Details

J General hospital and personal use equipment

J5200 Intravascular catheter

Imported from abroad

Dates and Status

Aug 22, 2013

Aug 22, 2018

Jan 15, 2020

Cancellation Information

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