Clinical Examination Universal Quality Control Substance I.
์์๊ฒ์ฌ๋ฒ์ฉ์ ๋๊ด๋ฆฌ๋ฌผ์งโ
This Unknown medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / ์ํ์์ฝํ์์ ์ฒ) under license number In Vitro Reception No. 19-2404. Approved on Sep 25, 2019. Registered by Biorad Korea Co., Ltd..
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
Unknown
Basic Information
Item Serial Number
2019005921
License Number
In Vitro Reception No. 19-2404
์ฒด์ธ์์ 19-2404ํธ
Classification Number
J08060.01
Device Class (Risk Classification)
Unknown
Classification Name
Clinical Examination Universal Quality Control Substance I.
์์๊ฒ์ฌ๋ฒ์ฉ์ ๋๊ด๋ฆฌ๋ฌผ์งโ
Official English Name
General calibrators, controls or standards, classโ
, for clinical chemistry
Company Information
Category
In vitro diagnostic import business
์ฒด์ธ์ง๋จ์์
์
Business License Number
์ฒด์ธ ์ 719 ํธ
Important Dates & Status
Item Approval Date
Sep 25, 2019
Business Permit Date
May 26, 2005
Expiration Period
2020-10-08 ~ 2030-09-30
Model Information
Model Name
12002594 Level 1 MiniPak

