Pure Global

“MediFirst” CATH PRO I.V Catheter - Taiwan Registration f8b00d5e8bceec1be98041e62ceed533

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 f8b00d5e8bceec1be98041e62ceed533 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
1 Recent Registrations
f8b00d5e8bceec1be98041e62ceed533
Registration Details
Taiwan FDA Registration: f8b00d5e8bceec1be98041e62ceed533
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

f8b00d5e8bceec1be98041e62ceed533

Ministry of Health Medical Device Import No. 032796

DHA05603279609

Company Information

Korea, Republic of

Product Details

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

J General hospital and personal use equipment

J5200 Intravascular catheter

Imported from abroad

Dates and Status

Aug 20, 2019

Aug 20, 2024

Companies Making Similar Products
Top companies providing products similar to "“MediFirst” CATH PRO I.V Catheter"