This document specifies the requirements and methods for the clinical investigation of ME equipment used to measure the body temperature in indirect measurement mode.
This document covers both intermittently and continuously measuring clinical thermometers.
NOTE For clinical thermometers in direct measurement mode determining the technical accuracy in accordance with IEC 80601-2-56 is typically sufficient.
This document specifies additional disclosure requirements.
This document is not applicable to the clinical investigation of a screening thermographs for human febrile temperature screening whose laboratory accuracy requirements are described in IEC 80601-2-59.
PROJEKAT
ISO 12487
60.00
Standard u postupku objavljivanja
30. 4. 2026.
Respiratorna oprema - Klinička ispitivanja kliničkih termometara
50.60 Završetak postupka odobravanja definitivnog teksta nacrta standarda