Company profile
PrimeMed Inc.
KO: (주)프라임메드
231
Total devices
2
Device classes
Jan 18, 2008
Earliest approval
Nov 13, 2023
Latest approval
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 |
About this profile
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 DatabasePowered by Pure Global AIMFDS Official Data231 Devices