Company profile
Dong Aesti Co., Ltd.
KO: 동아에스티(주)
308
Total devices
5
Device classes
Mar 02, 1998
Earliest approval
Dec 01, 2023
Latest approval
Device class distribution
Breakdown of 308 devices by regulatory classification
Unknown
202
65.6% of total
Class I
66
21.4% of total
Class III
20
6.5% of total
Class II
18
5.8% of total
Class IV
2
0.6% of total
Registered devices (10 most recent shown)
Click on any device for detailed registration information
| Device Name | Class | License Number | Approval Date |
|---|---|---|---|
| Electrocorporeal shock fracture crusher 전기체외충격파쇄석기 | Unknown | Suhe 23-383 | Dec 01, 2023 |
| Biomaterials for tissue repair 조직수복용생체재료 | Unknown | No. 23-700 | Jun 22, 2023 |
| Anti-adhesion cladding 유착방지피복재 | Unknown | No. 23-702 | Jun 22, 2023 |
| Thyroid function hormone test reagent 갑상선기능호르몬검사시약 | Class II | In vitro waters No. 22-4529 | Nov 10, 2022 |
| Cartridge syringe 카트리지형주사기 | Unknown | Suin 22-4220 | Apr 26, 2022 |
| Electrocorporeal shock fracture crusher 전기체외충격파쇄석기 | Class III | Suhe 21-309 | Dec 15, 2021 |
| Clinical Examination Universal Quality Control Substance I. 임상검사범용정도관리물질Ⅰ | Class I | In Vitro Reception No. 19-2127 | Aug 26, 2019 |
| Universal ultrasound imaging device 범용초음파영상진단장치 | Unknown | Suin No. 19-4335 | May 29, 2019 |
| Manual medical saws 수동식의료용톱 | Class I | Article 17-1425 | Dec 19, 2017 |
| Automatic medical separation method clinical chemistry analysis device 의료용분리방식임상화학자동분석장치 | Class I | In Vitro Reception No. 17-182 | Jan 19, 2017 |
About this profile
Complete regulatory portfolio for Dong Aesti Co., Ltd. in South Korea's medical device market. This company has 308 medical devices registered with South Korea MFDS, with registrations dating from Mar 02, 1998 to Dec 01, 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.
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