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DSHITECH Co., Ltd.

(์ฃผ)๋””์—์Šคํ•˜์ดํ…

Complete regulatory portfolio for DSHITECH Co., Ltd. in South Korea's medical device market. This company has 460 medical devices registered with South Korea MFDS, with registrations dating from Jan 15, 1999 to Jan 17, 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
460 Devices
Company Overview
Total Devices
460
Address
๊ฒฝ๊ธฐ๋„ ํ•˜๋‚จ์‹œ ์„œํ•˜๋‚จ๋กœ43๋ฒˆ๊ธธ 166 2์ธต (๊ฐ๋ถ๋™)
Registration Timeline
Earliest Approval
Jan 15, 1999
Latest Approval
Jan 17, 2023
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Device Class Distribution
Breakdown of 460 devices by regulatory classification
Class I
322
70.0% of total
Unknown
126
27.4% of total
Class II
9
2.0% of total
Class III
3
0.7% of total
Registered Devices (10 most recent shown)
Click on any device for detailed registration information