Taiwan FDA registration 0631c9234659ea29e2264e32a88aa600

“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 22, 2013 – Aug 22, 2018Cancelled
Registration details
Analysis ID
0631c9234659ea29e2264e32a88aa600
License Form
Ministry of Health Medical Device Import No. 025384
Customs Code
DHA05602538408
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
GREAT KUEI TAI INC.
Product details
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 22, 2013
Expiry Date
Aug 22, 2018
Cancellation Date
Jan 15, 2020
Cancellation information
Status
Logged out
Reason
自請註銷
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 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.

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