More info
Description / Abstract:
This standard, together with ISO 15004-1:2009, Fundamental
requirements and test methods – Part 1: General requirements
applicable to all instruments – First edition, specifies
minimum requirements and the design compliance procedure for
tonometers intended for routine clinical use in the estimation of
intraocular pressure (IOP) for the detection, diagnosis, and
management of ocular abnormalities.
NOTES
1) The true intraocular pressure is seldom directly measured
since it would require invasion of the eye. Since the true IOP
cannot be known, the instrument (annex A) and method (annex B) for
determining a reference IOP are established.
2) Clinical tonometers may employ different parameters or
correlates in the indirect assessment of measured IOP. The
manufacturer states the exact design parameters of the specific
tonometer, and then, on the basis of design compliance testing as
specified in 4.2, demonstrates that the specific design performs
acceptably compared to the reference method. This process is
referred to as certification.
The manufacturer also demonstrates, by methods specified in 4.3,
that individual manufactured instruments perform the same as
(within defined limits) the test tonometer. This process is
referred to as verification.