Eye dilator
๋ํ์ฅ๊ธฐ
This Class I medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / ์ํ์์ฝํ์์ ์ฒ) 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 Database
Powered by Pure Global AI
MFDS Official Data
Class I
Basic Information
Item Serial Number
2021001758
License Number
Reception No. 21-574
์์ 21-574ํธ
Classification Number
A59090.03(1)
Device Class (Risk Classification)
Class I
Classification Name
Eye dilator
๋ํ์ฅ๊ธฐ
Official English Name
Lacrimal duct dilator
Company Information
Entity Address
์์ธํน๋ณ์ ์ค๊ตฌ ์น ํจ๋ก 37 10์ธต (๋ด๋๋1๊ฐ)
Manufacturer
Rudischhauser Surgical Instruments Manufacturing GmbH
Category
Import business
์์
์
Business License Number
์ 3358 ํธ
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
์๋์ค
Model Information
Model Name
426090 and 1 other cases
426090์ธ 1๊ฑด
