Enzyme Immuno Assay (EIA), gonorrhea Ag, kit

Primary use
Diagnosis / Measurement / Monitoring
Type of medical device or related product
In vitro diagnostic tests
General vs. specific use (health condition)
Specific
Intended population age
Adolescent (10 to 19 years)
Adults (20 to 64 years)
Intended population sex
All
Level of technical knowledge
Specialized clinical
Capital
No
Reusable
Yes
Requirements
None
WHO list of priority medical devices
Reproductive, maternal, newborn and child health (2015)
Service delivery platforms / Healthcare levels
Second-level and third-level hospital services and specialized outpatient services
Healthcare unit
Laboratory
EMDN related code(s)
W0105010299
GONOCOCCI REAGENTS - OTHER
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
GMDN related code(s)
51231
Neisseria gonorrhoeae antigen IVD, kit, enzyme immunoassay (EIA) (A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of antigens from Neisseria gonorrhoeae bacteria, the causative agent of gonorrhoea, in a clinical specimen using an enzyme immunoassay (EIA) method.)
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 
Decommissioning
WHO resources on medical devices