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South Korea MFDS registration Reception No. 23-110

Medical Guide

KO: 의료용가이드
South KoreaClass ISmith & Nepew, Inc.Approved Jan 19, 2023
VerifiedMFDS · Ministry of Food and Drug Safety registry
Basic information
Item Serial Number
2023000349
License Number
Reception No. 23-110
수신23-110호
Classification Number
A64050.01(1)
Device Class (Risk Classification)
Class I
Classification Name
Medical Guide
의료용가이드
Official English Name
Guide for medical use
Company information
Entity Name (Company)
Smith & Nepew, Inc.
스미스앤드네퓨(주)
Entity Address
서울특별시 강남구 영동대로 517 , 13층 일부(삼성동, 아셈타워)
Category
Import business
수입업
Business License Number
제 360 호
Important dates & status
Item Approval Date
Jan 19, 2023
Business Permit Date
Mar 24, 2005
Expiration Period
2023-01-19 ~ 2028-01-18
For Export
아니오
Model information
Model Name
6 cases 42404211 and others
42404211외 6건
About this record

This Class I medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / 식품의약품안전처) under license number Reception No. 23-110. Approved on Jan 19, 2023. Registered by Smith & Nepew, Inc..

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 devices in South Korea.