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Company profile

Philips Korea Co., Ltd.

KO: (주)필립스코리아
South Korea서울특별시 중구 소월로2길 30 (남대문로5가)802 devicesRegistered Apr 06, 1998 – Dec 15, 2023
VerifiedMFDS · Ministry of Food and Drug Safety registry
802
Total devices
4
Device classes
Apr 06, 1998
Earliest approval
Dec 15, 2023
Latest approval
Regulatory footprint
Search Philips Korea Co., Ltd. across other regulatory registries
ThailandEuropean UnionColombiaCanadaEcuadorSaudi Arabia
Device class distribution
Breakdown of 802 devices by regulatory classification
Unknown63779.4% of total
Class I8710.8% of total
Class II486.0% of total
Class III303.7% of total
Registered devices (10 most recent shown)
Click on any device for detailed registration information
Patient Monitor
환자 감시장치
Dec 15, 2023
Class
Unknown
License Number
Suin 23-4911
Mobile X-ray fluoroscopy device
이동형엑스선투시촬영장치
Nov 13, 2023
Class
Unknown
License Number
Suhe 23-366
Magnetic Resonance Computed Tomography for Superconducting Magnet
초전도 자석식 전신용 자기공명 전산화 단층 촬영장치
Jun 30, 2023
Class
Unknown
License Number
Suin 23-4660
Universal ventilators
범용인공호흡기
Sep 02, 2022
Class
Unknown
License Number
Suhe 22-194
Endovascular sphygmomanometer
혈관내혈압계
Apr 27, 2022
Class
Class II
License Number
Suin No. 22-4224
In vitro medical electrodes
체외형의료용전극
Mar 28, 2022
Class
Class I
License Number
Reception No. 22-532
In vitro medical electrodes
체외형의료용전극
Mar 28, 2022
Class
Class I
License Number
Reception No. 22-530
In vitro medical electrodes
체외형의료용전극
Mar 28, 2022
Class
Class I
License Number
Reception No. 22-529
In vitro medical electrodes
체외형의료용전극
Mar 28, 2022
Class
Class I
License Number
Reception No. 22-528
In vitro medical electrodes
체외형의료용전극
Mar 28, 2022
Class
Class I
License Number
Reception No. 22-527
View all 802 devices →
About this profile

Complete regulatory portfolio for Philips Korea Co., Ltd. in South Korea's medical device market. This company has 802 medical devices registered with South Korea MFDS, with registrations dating from Apr 06, 1998 to Dec 15, 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.