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South Korea MFDS registration In Vitro Reception No. 23-2250

Medical immunofluorescence measurement device

KO: 의료용면역형광측정장치
South Korea flagSouth Korea·Unknown·Biomeriu Korea Co., Ltd.·Approved Sep 15, 2023
Basic information
Item Serial Number
2023005393
License Number
In Vitro Reception No. 23-2250
체외수신23-2250호
Classification Number
K01020.01
Device Class (Risk Classification)
Unknown
Classification Name
Medical immunofluorescence measurement device
의료용면역형광측정장치
Official English Name
Fluorimetric immunoassay analyzer(FIA), stationary
Company information
Entity Name (Company)
Biomeriu Korea Co., Ltd.
(주)비오메리으코리아
Category
In vitro diagnostic import business
체외진단수입업
Business License Number
체외 제 687 호
Important dates & status
Item Approval Date
Sep 15, 2023
Business Permit Date
May 24, 2005
Expiration Period
2023-09-15 ~ 2028-09-14
Model information
Model Name
KUBE LIVES
VIDAS KUBE
About this record

This Unknown medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / 식품의약품안전처) under license number In Vitro Reception No. 23-2250. Approved on Sep 15, 2023. Registered by Biomeriu Korea Co., Ltd..

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