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M Monitor Inc. is growing with
the aim of obtaining domestic market
and jumping up to global market.

2020

  • 02.Certified CE of Isopollo® H. pylori & ClaR
  • 02.Certified CE of Isopollo® Malaria (Pf/Pv) detection kit
  • 02.Launch of Isopollo® COVID-19 detection kit
  • 02.Medical device manufacturing report-
    Mmiso® ASFV detection kit
  • 02.First export to Russia
  • 03.Approval of manufacturing for export-
    Isopollo® Malaria detection kit(Pf,Pv)
  • 04.MOU with GCMS (Green Cross Medical Science Corp)
  • 10.Approval of manufacturing for export-
    MmaxSureTM SARS-CoV-2 Detection Kit
  • 11.Certified CE of MmaxSureTM SARS-CoV-2 Detection Kit
  • 12.Approval of manufacturing-
    Mmiso® ASFV detection kit(premix)

2019

  • 01.Medical device manufacturing report-
    Simple gene extraction reagent, Mmaxpress® DNA Kit HS2
  • 07.Approval of manufacturing, Isopollo® Dengue test kit
  • 09.Participation in the MFA 2019 (Medical Fair Asia 2019)
    exhibition
  • 10.Approval of manufacturing- Mmiso® FMDV pan detection kit
  • 11.Certified CE of Isopollo® Dengue test kit
  • 11.Participation in the Korean Society of
    Gastrointestinal Endoscopy
  • 11.Participation in the MEDICA in Dusseldorf, Germany
  • 12.Participation in the VIETNAM MEDI -PHARM EXPO
    2019 IN HANOI
  • 12.Start of ASFV detection kit clinical trial
  • 12.Medical device manufacturing report-
    Simple gene extraction reagent, Mmaxpress® prep kit HA01

2018

  • 12.MOU with INS, Peru
  • 11.Certified ISO 13485:2016
  • 10.Approval, launch of Isopollo® H.pylori & ClaR
  • 09.Approval, launch of Isopollo® Influenza A&B
    Completion of Mmiso® Dengue detection kit clinical trial
  • 08.Participation in the MFA 2018
    (Medical Fair Asia 2018) exhibition
  • 07.CDA with HSG, India
  • 05.Approval of manufacturing animal medical devices
    MOU with HSG, India
  • 03.MOU with Seoul CRO

2017

  • 12.2nd product clinical trial
  • 11.Permission of 1st product by Ministry of Food and Drug Safety
  • 09.Completion of 2nd production facility
  • 08.Completion of 1st product clinical trial
  • 04.Designated as a technology specialized company

2016

  • 11.Transfer Japan EIKEN Technology
  • 05.Medical device GMP facility approval
    by Ministry of Food and Drug Safety
  • 02.1st production facility completion

2014

  • 12.Certified Venture Company
  • 12.Certified Research Institute
  • 07.Start business