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This International Standard specifies requirements for a peak expiratory flow meter (pefm) intended for the assessment of pulmonary function in spontaneously breathing humans. This International Standard covers all medical devices that measure peak expiratory flowrate in...
This International Standard specifies requirements for a peak expiratory flow meter (pefm) intended for the assessment of pulmonary function in spontaneously breathing humans. This International Standard covers all medical devices that measure peak expiratory flowrate in...
This International Standard specifies requirements for a peak expiratory flow meter (pefm) intended for the assessment of pulmonary function in spontaneously breathing humans. This International Standard covers all medical devices that measure peak expiratory flowrate in...
This International Standard specifies requirements for a PEAK EXPIRATORY FLOW METER (PEFM) intended for the assessment of pulmonary function in spontaneously breathing humans. This International Standard covers all MEDICAL DEVICES that measure PEAK EXPIRATORY FLOWRATE in...
1.1 This test method covers measurement of resistance to plastic flow of 4 in. (102 mm) cylindrical specimens of asphalt mixture loaded in a direction perpendicular to the cylindrical axis by means of the Marshall apparatus. This test method is for use with dense-graded asphalt mixtures...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2017)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
The scope of this Recommendation1 is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a...
