Pure Global

DIO

(์ฃผ)๋””์˜ค

Complete regulatory portfolio for DIO in South Korea's medical device market. This company has 425 medical devices registered with South Korea MFDS, with registrations dating from Feb 28, 2003 to Dec 21, 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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MFDS Official Data
425 Devices
Company Overview
Total Devices
425
Address
๋ถ€์‚ฐ๊ด‘์—ญ์‹œ ํ•ด์šด๋Œ€๊ตฌ ์„ผํ…€์„œ๋กœ 66
Registration Timeline
Earliest Approval
Feb 28, 2003
Latest Approval
Dec 21, 2023
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Device Class Distribution
Breakdown of 425 devices by regulatory classification
Unknown
335
78.8% of total
Class I
61
14.4% of total
Class II
19
4.5% of total
Class III
10
2.4% of total
Registered Devices (10 most recent shown)
Click on any device for detailed registration information