ASTS Enterprises A310 User Manual
  1. Manuals
  2. Brands
  3. ASTS Enterprises Manuals
  4. Medical Equipment
  5. A310
  6. User manual

ASTS Enterprises A310 User Manual

Hide thumbs
Table of Contents

Advertisement

Quick Links

Model: A310
Pulse Oximeter
USER MANUAL
\
PLEASE NOTE:
THIS
MEDICAL INSTRUMENT MUST BE USED ACCORDING
TO INSTRUCTIONS TO ENSURE ACCURATE READINGS.
File No.: A310-OPE
V 1.3 202004
1 / 15

Advertisement

Table of Contents
loading
Need help?

Need help?

Do you have a question about the A310 and is the answer not in the manual?

Questions and answers

Summary of Contents for ASTS Enterprises A310

  • Page 1 Model: A310 Pulse Oximeter USER MANUAL PLEASE NOTE: THIS MEDICAL INSTRUMENT MUST BE USED ACCORDING TO INSTRUCTIONS TO ENSURE ACCURATE READINGS. File No.: A310-OPE V 1.3 202004 1 / 15...

  • Page 2: Section 1 Safety

     SpO2 measurements may be adversely affected in the presence of high ambient light. Shield the sensor area (with a surgical towel, or direct sunlight, for example) if necessary.  The following reason will cause interference to the testing accuracy of the A310 Pulse Oximeter .  High-frequency electrosurgical equipment.
  • Page 3 CAUTION: Keep the operating environment free of dust, vibrations, corrosive, or flammable materials, and extremes of temperature and humidity. CAUTION: Do not operate the unit if it is damp or wet because of condensation or spills. Avoid using the equipment immediately after moving it from a cold environment to a warm, humid location.

  • Page 4: Section 2 Introduction

    Section 2 Introduction 2.1 General This chapter provides a general description of the A310 Pulse Oximeter including:  Brief device description  Product features 2.2 Indication for use/ intended use The Pulse Oximeter is a non-invasive device intended for spot checking of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate (PR).
  • Page 5 CAUTION: A function tester cannot be used to assess the accuracy of a Pulse Oximeter monitor or sensor. Clinical testing is used to establish the SpO2 accuracy. The measured arterial SpO2 value (SpO2) of the sensor is compared to arterial hemoglobin oxygen(SaO2) value, determined from blood samples with a laboratory CO-oximeter.

  • Page 6: Section 3 Installation, Setup,And Operation

    Plethysmogram Battery Compartment 3.2 Display After switching on, the OLED display of the A310 Pulse Oximeter is as follows: Figure 3.2.1 OLED display 3.3 Parameter setting When the device is under measuring interface, press the direction button for 1 second in order to enter into menu page (figure 3.3.1 and figure 3.3.2).
  • Page 7 Press the direction button for 1 second, move the “*” symbol to the back of Sound Reminder, long press the direction button to turn it on/off. (Note: If the measured value exceeds the maximum or minimum value of SPO2 or PR, there will give off sound when sound reminder is turned on.) ...
  • Page 8 2.The customer can preset the limit value to the 98 or 99 to check whether it is normal for sound reminder setting. 3.If no sound reminder that includes the capability to detect an SpO2 or pulse rate PHYSIOLOGICAL SOUND REMINDER CONDITION is provided, a statement to that effect 4.The range of the peak wavelengths and maximum optical output power of the light emitted by the PULSE OXIMETER PROBE and a statement to the effect that information about...

  • Page 9: Section 4 Cleaning And Disinfection

    Note: 1. When battery power is at lowest level, the battery capacity indicates symbol of in OLED, remind users of replacement of battery. 2. The plethymogram can been regarded as correct if the wave is fluctuated regularly. Section 4 Cleaning and Disinfection 4.1 Cleaning Switch off the power and take out the batteries before cleaning.

  • Page 10: Section 5 Troubleshooting And Maintenance

    Section 5 Troubleshooting and Maintenance 5.1 Maintenance Replace the batteries timely when battery indication is low. Clean surface of the Pulse Oximeter before it is used in diagnosis for patients. Remove the batteries inside the battery cassette if the Oximeter will not be operated for a long time.

  • Page 11: Section 6 Specification

    Section 6 Specification Name Pulse Oximeter Model A310 Anti-electric Shock Type Internally powered equipment Anti-electric Shock Equipment Degree Type BF EMC Type Type B Class I Enclosure Degree of ingress protection IP22 Internal Power: 2xAAA 1.5v alkaline battery Power Consumption...
  • Page 12 Guidance and manufacturer´s declaration – electromagnetic immunity TheA310 Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the user of the A310 Pulse Oximeter should assure that it is used in such an environment. IEC 60601 Compliance...
  • Page 13 The A310 Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the user of the A310 Pulse Oximeter should assure that it is used in such an environment. Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance...
  • Page 14 If the measured field strength in the location in which the A310 Pulse Oximeter is used exceeds the applicable RF compliance level above, the A310 Pulse Oximeter should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the A310 Pulse Oximeter .

  • Page 15: Section 8 Disposal

    Listed with the Australian therapeutic good administration. ARTG identifier : 3183357. For information and warranty in Australia Please contact: ASTS Enterprises (AUST) Pty Ltd 2/11 Evans St, Burwood, VIC, 3125 +61 3 9888 8771 Fax: +61 3 9888 8220...

Table of Contents

Save PDF