Agilent Technologies Korea
ํ๊ตญ์ ์ง๋ฐํธํ
ํฌ๋๋ก์ง์ค(์ฃผ)
Complete regulatory portfolio for Agilent Technologies Korea in South Korea's medical device market. This company has 338 medical devices registered with South Korea MFDS, with registrations dating from Feb 04, 2009 to May 17, 2022.
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
338 Devices
Company Overview
Total Devices
338
Address
์์ธํน๋ณ์ ์์ด๊ตฌ ๊ฐ๋จ๋๋ก 369 , 13์ธต, 14์ธต
Registration Timeline
Earliest Approval
Feb 04, 2009
Latest Approval
May 17, 2022
Device Class Distribution
Breakdown of 338 devices by regulatory classification
Unknown
217
64.2% of total
Class I
118
34.9% of total
Class III
3
0.9% of total
Registered Devices (10 most recent shown)
Click on any device for detailed registration information