Pure Global

Baxter Inc.

(์ฃผ)๋ฐ•์Šคํ„ฐ

Complete regulatory portfolio for Baxter Inc. in South Korea's medical device market. This company has 253 medical devices registered with South Korea MFDS, with registrations dating from Oct 02, 1998 to Feb 02, 2024.

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
253 Devices
Company Overview
Total Devices
253
Address
์„œ์šธํŠน๋ณ„์‹œ ์ข…๋กœ๊ตฌ ์ข…๋กœ 1 10์ธต 1001ํ˜ธ (์ข…๋กœ1๊ฐ€, ๊ต๋ณด์ƒ๋ช…๋นŒ๋”ฉ)
Registration Timeline
Earliest Approval
Oct 02, 1998
Latest Approval
Feb 02, 2024
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Device Class Distribution
Breakdown of 253 devices by regulatory classification
Unknown
177
70.0% of total
Class II
39
15.4% of total
Class III
22
8.7% of total
Class I
8
3.2% of total
Class IV
7
2.8% of total