# Welcome

​ ​ Momo is a Microbiological Analytics and Clinical Tool for Reporting Pathogens and Antimicrobial Resistances ​ ​

Momo (Monitoring of Microorganisms) provides all the information on pathogen occurrence, frequency distribution and resistance situation in one place. 59 different parameters allow maximum flexibility for clinical, QM, and administrative queries. User-defined templates facilitate reporting and benchmarking. ​

Momo has a strong clinical feature:
Momo's QuickScan gives immediate single patient overviews with all or all positive, approved results for one patient. It serves as a fast clinical tool for the attending physician and is always up-to-date. ​

Momo accommodates all data items available in modern microbiological laboratories: bacteria and fungi including AMR profiles, PCR results, serology results, toxins, microscopy results, remarks, and miscellaneous others. ​

  • QuickScan: Get single patient overviews with just one click using this fast clinical tool. Choose only positive, approved or all results. ​
  • FlexScan: Use these highly customizable queries that can access all available microbiological data. Answer clinical, epidemiological, and QM questions with our 59 query parameters. ​
  • Spectrum: Based on a FlexScan or QuickScan result, Spectrum analyzes the data and provides frequency distributions for each or for a combination of selected parameters. ​
  • AMR: Click amr-create in your Spectrum results to receive the complete antimicrobial resistance situation for every found pathogen and have it graphically displayed. ​
  • OneClick: At the point of care, Momo’s QuickScan reports can directly be accessed with only one click from PDMS or AKIM in a password-less authentication process. ​ ​ ​


The attending physician alone is responsible for the patient's diagnosis and therapy. Only the doctor will be able to align the statistical data displayed by Momo with the full clinical picture of the patient.
In May 2022 Momo received a declaration of conformity for the EU IVD Directive 98/79/EC. It is now a declared medical device and CE (Conformité Européenne) marked, indicating that it complies with all EU standards for health and safety.