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General| Category | Medical Equipment |
|---|---|
| Cuff Size | 22-32cm |
| Type | Blood Pressure Monitor |
| Measurement Method | Oscillometric |
| Accuracy | ±3 mmHg (Pressure), ±5% (Pulse) |
| Display | LCD |
Identifies the product model, name, and manufacturer.
Provides contact details for after-sales support and service inquiries.
Lists document number, revision version, and release date.
Details the CE mark certification and the designated EC representative.
Outlines the copyright ownership and terms of use for the manual.
Specifies conditions under which the manufacturer is responsible for the instrument.
Explains the manual's purpose and the importance of following its instructions.
Clarifies that content may vary by configuration and illustrations are examples.
Explains special text formatting and symbols used in the manual.
Defines the meaning of Warning, Caution, and Note symbols and their implications.
Specifies the intended purpose and application areas of the pulse oximeter.
Describes the components and controls on the front panel of the oximeter.
Identifies the components located on the rear panel of the oximeter.
Details the connectors and ports found on the side of the oximeter.
Explains the display layout when showing large numerical values for SpO2 and PR.
Describes the display layout when showing the SpO2 waveform and associated data.
Provides crucial safety warnings regarding device usage, environment, and general precautions.
Explains the meaning of various symbols used throughout the manual for clarity.
Guides the user on how to unpack and verify the contents of the package upon receipt.
Details how to adjust the volume of audible beeps from the device for user preference.
Guides on adjusting button press volume and screen brightness for optimal usability.
Describes how to configure the scan speed for measurements according to user needs.
Details the functionality and use of the continuous monitoring mode for long-term patient observation.
Describes the features and operation of the spot-checking mode for short-term measurements.
Explains how to select the patient type (Adult, Pediatric, Neonate) for appropriate settings.
Provides instructions for using and exiting the device's demonstration mode for familiarization.
Outlines steps for changing language and checking the device software version.
Guides the user on how to reset the oximeter to its default factory settings.
Classifies the types of alarms the oximeter can generate for alerts.
Explains the meaning of low, medium, and high alarm levels for physiological alarms.
Describes the audible tones used for different alarm levels, indicating severity.
Explains the visual indications provided by the alarm lamp for different severity levels.
Details alarm text messages, colors, and flashing numeric indicators for alarm events.
Guides on setting minimum and general alarm volume levels for audible alerts.
Emphasizes checking the patient's condition first when an alarm sounds for prompt assessment.
Provides a step-by-step guide on how to respond to and resolve alarm events.
Introduces the principles and method of measuring oxygen saturation using light spectra.
Lists safety warnings for SpO2 sensors, including checks, handling, and disposal.
Lists crucial warnings related to sensor placement and conditions during monitoring.
Explains how to enable or disable SpO2 alarms for customized monitoring.
Describes how to set the severity level (low, medium, high) for SpO2 alarms.
Details how to set the high and low limits for SpO2 alarms to trigger alerts.
Explains how to adjust the desaturation limit for SpO2 alarms to tailor alert sensitivity.
Explains how to enable or disable PR alarms for customized monitoring.
Describes how to set the severity level (low, medium, high) for PR alarms.
Details how to set the high and low limits for PR alarms to trigger alerts.
Introduces the feature for reviewing previously stored SpO2 and PR data trends.
Explains the display interface for reviewing stored SpO2/PR data and its components.
Details options for trend setup including interval, ID selection, data deletion, and export.
Introduces the battery types supported and general maintenance requirements for the oximeter.
Explains how the battery icon indicates the remaining power level and low battery warnings.
Details the steps required to open the battery compartment door for battery access.
Guides on correctly inserting alkaline AA batteries into the device, noting polarity.
Explains how to install the rechargeable Lithium-Ion battery into the device, ensuring proper fit.
Outlines general rules for maintaining and cleaning the oximeter to prevent damage and ensure longevity.
Lists specific electrical safety tests and leakage current checks for annual device verification.
Lists available Nellcor SpO2 sensor models and their applicable patient categories for selection.
Lists safety-related technical classifications and certifications for the device, such as SFDA and CE.
Details the type, size, and resolution of the device's OLED display.
Specifies the types, colors, and behavior of indicating LEDs on the mainframe and charger.
Specifies audio output capabilities, including alarm and beep tones, and their pressure levels.
Lists the quantity and functional descriptions of the device's control buttons.
Describes the technical specifications of the pulse oximetry sensors, including emission wavelengths.
Details how trend data is displayed, the interval, and storage capacity for different modes.
Provides detailed measurement specifications for SpO2, including range, resolution, and accuracy.
Details measurement specifications for Nellcor SpO2 technology, including accuracy for different patient types.
Specifies the ranges and steps for setting SpO2 and PR alarm limits to trigger alerts.
Continues the specifications for PR alarm limit ranges and steps for setting alerts.
Provides declarations and guidance regarding electromagnetic emissions from the device as per standards.
Specifies recommended separation distances for RF communication equipment to maintain EMC compliance.
Provides tables for separation distances based on transmitter output power and frequency to prevent interference.
Lists the factory default settings for alarm configurations like volume and levels.
Lists the factory default settings for system configurations like beep volume and brightness.
Lists the factory default SpO2 and PR alarm limits for different patient types.
Lists the factory default setting for the trend interval parameter.
Lists physiological alarm messages, their causes, and corresponding severity levels.
Lists technical alarm messages, their causes, and corresponding severity levels.
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