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Disease/health condition - Meningitis
Discipline - Clinical microbiology
Antibacterial susceptibility testing
Setting:
2. Laboratory
Tiered Testing Service:
District hospital with laboratory Regional or provincial hospital with laboratory
Assay format
Automated systems
Information History
First added in 2020
Changed in 2024
Purpose type
Aid to diagnosis
Purpose
Final step in selection of appropriate antibiotics after species identification and interpretation by EUCAST and CLSI guidelines.
Specimen types
Bacterial isolates
WHO prequalified or recommended products
N/A
GMDN

56737

Antimicrobial susceptibility analyser IVD

An electrically-powered automated or semi-automated laboratory instrument intended to be used for the in vitro determination of an antimicrobial susceptibility profile by monitoring the growth rate of a microbiological organism from a clinical specimen and/or culture isolate when exposed to a range of antimicrobials. Growth detection technology used may include immunoassay, colorimetry, chromatography, photometric and/or carbon dioxide production.

The medical device term(s), code(s) and definition(s) in this section were retrieved from databases external to WHO. As there might be more than one name, definition and “Nomenclature Code” related to the specific medical device, please consult https://gmdnagency.org GMDN ®. © GMDN Agency 2005-2024
EMDN

W01040801

BIOCHEMICAL IDENTIFICATION AND SUSCEPTIBILITY TESTING - AUTOMATED

The code(s) and term(s) in this section were observed and retrieved from public databases and have not been validated by health regulatory authorities. Please consult your regulatory agency and EMDN site: https://webgate.ec.europa.eu/dyna2/emdn
WHO supporting publications
World Health Organization. (‎2025)‎. WHO guidelines on meningitis diagnosis, treatment and care. World Health Organization. https://iris.who.int/handle/10665/381006
Technical specifications
N/A
Related Medical Devices in MeDevIS
SAGE IVD recommended including this test in the EDL on the basis of the scientific validity of the analyte. It was recognized that the test is a foundational IVD test and is included in clinical guidelines.
N/A
The inclusion of this test was based on WHO guidelines and/or technical documents that include recommendations for the use of this test.
N/A