Taiwan FDA registration f8b00d5e8bceec1be98041e62ceed533

“MediFirst” CATH PRO I.V Catheter

TW: “美德芙”靜脈留置針
Taiwan flagTaiwan·Risk Class 2·MD·MediFirst Co., Ltd.·Registered Aug 20, 2019 – Aug 20, 2024Expired
Registration details
Analysis ID
f8b00d5e8bceec1be98041e62ceed533
License Form
Ministry of Health Medical Device Import No. 032796
Customs Code
DHA05603279609
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
GREAT KUEI TAI INC.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J5200 Intravascular catheter
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 20, 2019
Expiry Date
Aug 20, 2024
Companies making similar products

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

Recent registrations

Recently registered similar products

About this record

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 DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations