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Omron BP9300T - Page 37

Omron BP9300T
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37
Note
These specifications are subject to change without notice.
This monitor is clinically investigated according to the requirements of
ISO 81060-2:2013 and complies with ISO 81060-2:2013 and
ISO 81060-2:2018+A1:2020. In the clinical validation study, K5 was used on
85 subjects for determination of diastolic blood pressure.
This monitor has not been validated for use on pregnant patients.
IP classification is degrees of protection provided by enclosures in accordance
with IEC 60529. This monitor and optional AC adapter are protected against solid
foreign objects of 0.5 inch (12.5 mm) diameter and greater such as a finger.
The optional AC adapter is protected against vertically falling water drops which
may cause issues during a normal operation.
Operation mode classification complies with IEC 60601-1.
Storage / Transport
conditions
-4 °F to +140 °F (-20 °C to +60 °C) / 10 to 90 % RH
(non-condensing)
Weight
Monitor: Approximately 8.8 oz. (250 g) not including
batteries
Arm cuff: Approximately 6 oz. (170 g)
Dimensions
Monitor: Approximately 4.1" (w) × 3.2" (h) × 5.5" (l)
(103 mm × 82 mm × 140 mm)
Arm cuff: Approximately 5.7" × 23.4" (air tube: 29.5")
(145 mm × 594 mm (air tube: 750 mm))
Cuff circumference
applicable to the monitor
7" to 17" (17 to 42 cm) (included arm cuff: 9" to 17"
(22 to 42 cm))
Memory Stores up to 30 readings
Contents
Monitor, Wide-Range D-Ring Cuff, 4 “AA” batteries,
instruction manual, quick start guide
Protection against
electric shock
Internally powered ME equipment (When using only
batteries)
Class II ME equipment (Optional AC adapter)
Applied part Type BF (arm cuff)

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