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South Korea MFDS registration In Vitro Reception No. 22-1709

Centrifuge for cells

KO: 세포용원심분리장치
South Korea flagSouth Korea·Unknown·Abbott Korea·Approved Oct 07, 2022
Basic information
Item Serial Number
2022005106
License Number
In Vitro Reception No. 22-1709
체외수신22-1709호
Classification Number
I01030.01
Device Class (Risk Classification)
Unknown
Classification Name
Centrifuge for cells
세포용원심분리장치
Official English Name
Centrifuge, low-/medium-speed, cytological
Company information
Entity Name (Company)
Abbott Korea
한국애보트(유)
Category
In vitro diagnostic import business
체외진단수입업
Business License Number
체외 제 371 호
Important dates & status
Item Approval Date
Oct 07, 2022
Business Permit Date
Mar 30, 2005
Expiration Period
2022-10-07 ~ 2027-10-06
Model information
Model Name
Centrifuge GLP Z500
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. 22-1709. Approved on Oct 07, 2022. Registered by Abbott Korea.

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