What to do if nothing appears on my A&D UM-102 display?
If nothing appears on the display of your A&D Blood Pressure Monitor, even when you turn it on, the batteries may be empty. Replace all batteries with new ones. Also, ensure the battery polarities are correctly aligned. Reinstall the batteries, matching the positive and negative ends to the markings in the battery compartment.
Why is the cuff not inflating on my A&D UM-102?
If the cuff on your A&D Blood Pressure Monitor isn't inflating, it could be due to a few reasons. First, check the air hose connection and make sure the cuff and air hose are properly connected, without any twists in the hose. Second, there may be air leaking from the cuff or rubber bulb. If this is the case, replace the cuff or rubber bulb with a new one.
General| Type | Upper Arm Blood Pressure Monitor |
|---|---|
| Measurement Method | Oscillometric |
| Display | LCD |
| Cuff Size | 22-32 cm |
| Memory | 60 readings |
| Inflation | Automatic |
| Deflation | Automatic |
| Measurement Range (Blood Pressure) | 0-299 mmHg |
| Accuracy (Blood Pressure) | ±3 mmHg |
| Irregular Heartbeat Detection | Yes |
| WHO Blood Pressure Classification Indicator | Yes |
| Arm | Upper Arm |
| Measurement Range (Pulse) | 40-180 beats per minute |
| Accuracy (Pulse) | ±5% |
| Power Source | 4 x AA batteries or AC adapter (optional) |
| Weight | Approx. 300g (excluding batteries) |
Device for individuals skilled in blood pressure measurement via auscultation.
Suitable for adults and children aged 3 years and older.
Designed for operation within a medical facility setting.
To measure human blood pressure and heart rates.
Monitors cuff pressure during inflation/deflation for manual blood pressure determination.
Mercury-free design with automatic quick exhaust valve for patient safety.
Conforms to EU Directive 93/42 EEC for Medical Products, marked with CE0123.
Defines essential terms like SYS, DIA, PUL, Exhaust, and Constant exhaust.
Guidelines for using, mixing, storing, and expected battery life for LR6/AA batteries.
Instructions for immediate cessation of use and preventing further misuse.
Advises against self-repair; contact authorized dealers for service or replacement.
Advises against use with blood flow disorders or during abnormalities.
Lists situations where device use is prohibited, like ambulances or unhealed wounds.
Avoid water, high temperatures, humidity, direct sunlight, and vibration.
Ensure correct function, connections, cleanliness, and placement away from interference.
Monitor patient status, handle device with care, and avoid battery contact issues.
Includes cleaning the device, turning it off, and proper storage of accessories.
Recommends periodic checks and professional calibration for accuracy.
Ensures patient relaxation, proper cuff placement, and stillness during measurement.
Considers patient position, posture, movement, and emotional state for accurate results.
Details parts like displays, buttons, air hose, cuff, and accessories.
Explains the meaning of various symbols and readings shown on the device's LCD.
Covers symbols for power, battery, error codes, units, and regulatory labels.
Step-by-step guide for inserting and replacing batteries, with important cautions.
Instructions on securely inserting the air hose into the cuff connector.
Procedure for connecting the air hose socket to the main body's cuff connector.
Guidance on cuff selection based on arm circumference for accurate readings.
Instructions for wrapping the cuff around the arm at the correct position.
Explains symbols printed on the cuff, including fit range and artery position.
Details cuff placement, button presses, inflation, and stethoscope use.
Conditions for displaying heart rate after measurement completion.
Procedures for releasing cuff air and interpreting error messages like 'Err'.
How to turn off the device and information on its automatic power-off function.
How to mark specific pressure values during the measurement process.
Explains the function and display of the device's usage hour counter.
Lists common problems, their causes, and recommended actions for resolution.
Detailed instructions for cleaning the device and cuff with approved disinfectants.
Guidance on disposing of the unit and batteries according to local environmental regulations.
Includes model, measurement ranges, power, cuff sizes, and useful life.
Details emission limits and immunity test levels for RF wireless communications equipment.
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