Technical Specification - HEINE GAMMA G5 Manual De Instrucciones

changing the position of the spoon (GAMMA G5, G7, GP)
The spoon is normally set for right-handed use. If you wish to inflate the cuff with the left hand, the spoon can be
re-positioned for left-handed use:
• Remove the ball from the instrument with a twisting and pulling motion.
• Loosen the two screws near the air intake but do not screw them out completely.
(A special tool is supplied with GAMMA G7 for this purpose).
• Rotate the base of the spoon through 180° and re-tighten the screws.
• Grip the neck of the ball and push it back onto the air intake with a twisting motion. If necessary moisten the air
intake to ease fitting.
HyGIENIc cLEANING / PROcESSING
The following recommendations must be followed in procedures in hospitals / practises with regard to national
hygienic guidelines and / or legal requirements.
Manual cleaning
Clean all accessible surfaces by wiping with a damp cloth (water, pH-neutral, light alkaline detergent). The cuff
could be hand washed at 30 °C after removing the bladder.
Manual Disinfection
Do a cleaning disinfection of all accessible surfaces by wiping with a damp cloth. For disinfection only those
products which are approved for use on medical devices made of plastic and aluminium alloy (GAMMA G7)
may be use. The manufacturer's recommendations must be followed.
Sphygmomanometer:
Liquid must not penetrate the device. Disinfection by spraying and soaking is not allowed.
Cuff / Bladder:
Cuff and Bladder are released to for a disinfection by spraying and soaking.
Machine cleaning / Ultrasonic cleaning / Sterilisation
Sphygmomanometer, cuff and bladder are not permitted for these procedures as they will lead to damage of the
components.
Maintenance
This product does not require regular maintenance.
Service
This product does not require regular service.

technical specification

Range:
Accuracy:
Environmental conditions:
Normal Use:
Storage:
Relative humidity:
Note calibration: A calibration check should be carried out at the latest every two years by the manufacturer or
an authorized service technician.
Applicable standards:
DIN EN 1060: "Non-invasive sphygmomanometers" ,
Part 1: General requirements, and
Part 2: Supplementary requirements for mechanical sphygmomanometers
ANSI/AAMI SP9: 1994
ANSI/AAMI/ISO 81060-1:2007
Disposal
The product must be recycled as separated electrical and electronic devices. Please observe the relevant
state-specific disposal regulations.
0 – 300 mmHg
± 3 mmHg
0°C to +40°C
-34°C to +70°C
≤ 85%
med 0708 2014-02-12
7/32