PrimeMed Inc.

(주)프라임메드

Complete regulatory portfolio for PrimeMed Inc. in South Korea's medical device market. This company has 231 medical devices registered with South Korea MFDS, with registrations dating from Jan 18, 2008 to Nov 13, 2023.

Browse the complete device portfolio including device classifications, license numbers, approval dates, and technical specifications. Pure Global AI provides free access to comprehensive South Korea MFDS registration data, helping global MedTech companies analyze market presence and regulatory compliance for medical device manufacturers in South Korea.

Free Database

MFDS Official Data

231 Devices

Company Overview

Total Devices

231

Address

경기도 성남시 수정구 성남대로 1244 , 107 (태평동, 인티움)

Registration Timeline

Earliest Approval

Jan 18, 2008

Latest Approval

Nov 13, 2023

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Class Distribution

Breakdown of 231 devices by regulatory classification

Unknown

127

55.0% of total

Class I

104

45.0% of total

Registered Devices (10 most recent shown)

Click on any device for detailed registration information

Device Name	Class	License Number	Approval Date
Reusable medical forceps 재사용가능 의료용 겸자	Unknown	Reception No. 23-2612	Nov 13, 2023
Bone forceps 골겸자	Class I	Reception No. 23-130	Jan 25, 2023
Reusable universal manual medical clamp 재사용가능범용수동식의료용클램프	Unknown	Reception No. 22-1390	Aug 11, 2022
Aspiration tube and catheter 흡인용튜브·카테터	Class I	Reception No. 22-1312	Jul 27, 2022
Reusable manual medical scissors 재사용가능수동식의료용가위	Class I	Reception No. 22-1223	Jul 13, 2022
Bone forceps 골겸자	Unknown	Reception No. 22-1210	Jul 12, 2022
Reusable manual medical curette 재사용가능수동식의료용큐렛	Class I	Reception No. 22-1190	Jul 11, 2022
Manual Medical Stripper 수동식의료용스트리퍼	Unknown	Reception No. 22-1195	Jul 11, 2022
Manual osteoderm 수동식절골기	Unknown	Reception No. 22-1194	Jul 11, 2022
Manual vasodilator 수동식혈관확장기	Class I	Reception No. 22-840	May 12, 2022