South Korea MFDS registration Reception No. 21-574

Eye dilator

KO: 눈확장기
South Korea flagSouth Korea·Class I·Teleflex Korea·Approved Apr 06, 2021
Basic information
Item Serial Number
2021001758
License Number
Reception No. 21-574
수신21-574호
Classification Number
A59090.03(1)
Device Class (Risk Classification)
Class I
Classification Name
Eye dilator
눈확장기
Official English Name
Lacrimal duct dilator
Company information
Entity Name (Company)
Teleflex Korea
텔레플렉스코리아(유)
Entity Address
서울특별시 중구 칠패로 37 10층 (봉래동1가)
Manufacturer
Rudischhauser Surgical Instruments Manufacturing GmbH
Category
Import business
수입업
Business License Number
제 3358 호
Important dates & status
Item Approval Date
Apr 06, 2021
Business Permit Date
Jun 19, 2014
Expiration Period
2021-04-06 ~ 2026-04-05
For Export
아니오
Model information
Model Name
426090 and 1 other cases
426090외 1건
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. 21-574. Approved on Apr 06, 2021. Registered by Teleflex 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