Teleflex Korea
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๋ ํ๋ ์ค์ฝ๋ฆฌ์(์ )
Complete regulatory portfolio for Teleflex Korea in South Korea's medical device market. This company has 328 medical devices registered with South Korea MFDS, with registrations dating from Aug 05, 2002 to Dec 16, 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
328 Devices
Company Overview
Total Devices
328
Address
์์ธํน๋ณ์ ์ค๊ตฌ ์น ํจ๋ก 37 10์ธต (๋ด๋๋1๊ฐ)
Registration Timeline
Earliest Approval
Aug 05, 2002
Latest Approval
Dec 16, 2022
Device Class Distribution
Breakdown of 328 devices by regulatory classification
Class I
140
42.7% of total
Unknown
131
39.9% of total
Class II
38
11.6% of total
Class III
11
3.4% of total
Class IV
8
2.4% of total
Registered Devices (10 most recent shown)
Click on any device for detailed registration information