HomeKorea, RepublicMedifirst Co., Ltd.

Medifirst Co., Ltd.

Korea, Republic · Cheonan-Si Chungnam
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Israel, Russia — 4 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
5listed device types
Class I 1Class II 3Class III 0unclassified 1
plus 5 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
RURussiaRoszdravnadzor
2active registrations
Class 3 2
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States5 registration records, 1 510(k), 0 PMA
Brazil2 confirmed, 20 excluded
Manufacturer names merged into this page: Medifirst Co.,Ltd. · MEDI FIRST CO. LTD

Company information

Country
Korea, Republic
City
Cheonan-Si Chungnam

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12020 · K192230

FDA listed device types

Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua 1Needle, Hypodermic, Single Lumen 1Syringe, Piston 1Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days 1Container, Specimen Mailer And Storage, Sterile 1

Registration details (sample)

MarketIdentifierNameClass / date
USK192230MF SAFECATH2020-04-23
BR10390380006CATETERES DESCARTÁVEIS MF CATH PROClass II
BR80245210151CREMER INVENA - Cateter Intravenoso Periférico EstérilClass II

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