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ANSI Z80.10

Ophthalmics Ophthalmic Instruments – Tonometers

Organization:
ANSI - American National Standards Institute
Year: 2014

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.
URI: http://mapnamagz.yabesh.ir/std;query=authoF23793FD08/handle/yse/80808
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contributor authorANSI - American National Standards Institute
date accessioned2017-09-04T16:17:26Z
date available2017-09-04T16:17:26Z
date copyright2014.12.05
date issued2014
identifier otherTCRWJFAAAAAAAAAA.pdf
identifier urihttp://mapnamagz.yabesh.ir/std;query=authoF23793FD08/handle/yse/80808
description abstractThis 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.
languageEnglish
titleANSI Z80.10num
titleOphthalmics Ophthalmic Instruments – Tonometersen
typestandard
page25
statusActive
treeANSI - American National Standards Institute:;2014
contenttypefulltext
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