Preferred Label : Testing of Device from Other Lot/Batch Retained by Manufacturer;
Alternative definition : FDA: The investigation employed relevant empirical testing of the device of another
lot or batch than that of the suspected device in the reported adverse event in order
to support the identification of possible causes for the adverse event. This includes
devices without a lot/batch designation. Testing was performed using the device retained
by the manufacturer (i.e. was not shipped). Relevant testing would typically be based
on test methods used for evaluating safety and performance as described in the latest
relevant standards.;
NCI Metathesaurus CUI : CL526778;
Codes from synonyms : 4102;
Origin ID : C139448;
UMLS CUI : C4528480;
Automatic exact mappings (from CISMeF team)
- Semantic type(s)
- concept_is_in_subset
