South Korea MFDS registration Reception No. 23-292

Reusable endoscopic forceps

KO: 재사용가능내시경겸자
South Korea flagSouth Korea·Class I·Asrex Korea·Approved Feb 20, 2023
Basic information
Item Serial Number
2023000902
License Number
Reception No. 23-292
수신23-292호
Classification Number
A31010.29(1)
Device Class (Risk Classification)
Class I
Classification Name
Reusable endoscopic forceps
재사용가능내시경겸자
Official English Name
Endotherapy forceps, reusable
Company information
Entity Name (Company)
Asrex Korea
아스렉스코리아(유)
Entity Address
서울특별시 강남구 테헤란로 521 20층(삼성동)
Category
Import business
수입업
Business License Number
제 4030 호
Important dates & status
Item Approval Date
Feb 20, 2023
Business Permit Date
Feb 13, 2017
Expiration Period
2023-02-20 ~ 2028-02-19
For Export
아니오
Model information
Model Name
AR-13971W and 2 others
AR-13971W외 2건
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. 23-292. Approved on Feb 20, 2023. Registered by Asrex Korea.

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.

Free DatabasePowered by Pure Global AIMFDS Official DataClass I