gimaitaly KM-221 Blood Pressure cuff

Introduction
Product name: Blood Pressure Cuff
Product model and configuration: KM series (reusable cuff):
| Model | Applicable to | Application site | Limb circumference |
| KM-221 | Infant |
Arm | 6cm – 11cm |
| KM-222 | Infant | 8cm – 13cm | |
| KM-232 | Child | 10cm – 19cm | |
| KM-233 | Child | 18cm – 26cm | |
| KM-241 | Adult | 21cm – 35cm | |
| KM-242 | Adult | 27cm – 42cm | |
| KM-243 | Adult | 40cm – 48cm | |
| KM-244 | Adult | Thigh | 46cm – 66cm |
| KM-333 | Child |
Arm | 18cm – 26cm |
| KM-341 | Adult | 21cm – 35cm | |
| KM-342 | Adult | 27cm – 42cm | |
| KM-343 | Adult | 40cm – 48cm |
Service life: 2 years
KN series (reusable cuff):
| Model | Applicable to | Application site | Limb circumference |
| KN-221 | Infant |
Arm | 6cm – 11cm |
| KN-231 | Child | 10cm – 19cm | |
| KN-233 | Child | 18cm – 26cm | |
| KN-241 | Adult | 25cm – 35cm | |
| KN-243 | Adult | 33cm – 47cm | |
| KN-244 | Adult | Thigh | 46cm – 66cm |
Intended use: The blood pressure cuff is indicated for use in manual measurement and automatic non- invasive blood pressure monitoring. It’s applicable to be used with a compatible monitor
Instructions for use
- Appropriate cuff should be selected according to the age and arm/thigh circumference of the subject. Its width should be 2/3 of the length of the upper arm/thigh. The inflatable part should be long enough to permit wrapping approximately 80% of the limb. When cuff sizes overlap for a specified circumference, choose the larger size.
- Check the cuff before use, replace the cuff when aging, tearing or weak closure is apparent. Do not use a damaged cuff. Select the appropriate blood pressure measurement site. Inspect patient’s limb prior to application.
- When applying the cuff, unfold and wrap around the upper arm/thigh evenly to the appropriate tightness.
- The cuff should be tightened to a degree where insertion of one finger is allowed
- Locate the cuff in such a way that the artery mark is at a location where the clearest pulsation of brachial artery is observed.
- Remember to empty any residual air in the cuff before the measurement is commenced.
Operating Environment
Ambient temperature range: -10℃~ 40℃; Relative humidity: 10%~85%; Atmospheric pressure: 50kPa ~106.0kPa The cuff should be stored and used within the specified temperature and humidity range, or it may cause damage to the cuff or inaccurate measurement results.
Cleaning and Disinfection
- Prepare the enzymatic detergent or equivalent and distilled water, and 10% bleach solution in separate spray bottles.
- Spray detergent liberally on cuff, tubing and hose. If dirt is dried on, allow the detergent to soak in to the cuff for one minute.
- Wipe smooth surface with a soft cloth. Use a soft-bristle brush on visibly stained areas and irregular surfaces. Note: Take particular care when cleaning the bulb and control valve knob on a complete inflation system. Do not allow fluid to enter back valve or saturate control valve knob. Remove visible contaminants from the periphery and the underside of the control valve knob.
- Rinse with copious amounts of distilled water.
- To disinfect, spray 10% bleach solution on cuff until saturated and allow to soak for five minutes.
- Wipe away excess solution and rinse again with distilled water. Allow cuff to air dry
Warnings and Precautions
- Blood pressure measurement is prohibited to those who have severe hemorrhagic tendencies or with sickle cell disease, as partial bleeding may be caused.
- Continuous measurement may result in purpura, neuralgia and lack of blood.
- Do not place the cuff on limbs with transfusion tubes, intubations or skin lesions on the area, as damage may be caused to the limbs.
- Avoid compressing or restricting the connection tubing.
- Minimize limb movement and cuff motion during measurement.
- Check the site and limb frequently, especially when monitoring at frequent intervals and/or over extended periods of time.
- Remove the cuff from the patient when the measurement has been taken.
- Use cuff only under direct supervision by trained healthcare professional when attached to automated monitors without alarms.
- Before use, empty the cuff until there is no residual air inside.
- Do not allow the cuff to twist or bend. Do not twist the cuff hose or put heavy things on it.
- Please hold the connector of the hose while connecting and disconnecting it to the device.
- If arrhythmia or auricular fibrillation occurs, take the measurement again.
- Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the
- Member State in which the user and/or patient is established.
![]() | Medical Device compliant with Regulation (EU) 2017/745 | Product code | |
![]() | Manufacturer | ![]() | Authorised representative in the European Community |
![]() | Medical device | ![]() | Caution: read instructions (warnings) carefully |
![]() | Follow instructions for use | ![]() | Date of manufacture |
![]() | Temperature limit | ![]() | Humidity limit |
![]() | Atmospheric pressure limit | ![]() | Expiration date |
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