Microlife Aponorm Basis Control - Using the Mains Adapter; Connecting the Mains Adapter; Mains Operation Benefits

aponorm
®
Basis Control
19
EN
Device care
Clean the device only with a soft, dry cloth.
Cleaning the cuff
Carefully remove spots on the cuff with a damp cloth and
soapsuds.
WARNING: Do not wash the cuff in a washing machine
or dishwasher!
Accuracy test
We recommend this device is tested for accuracy every 2 years
or after mechanical impact (e.g. being dropped). Please contact
aponorm
®
by microlife-Service to arrange the test (see
foreword).
Disposal
Batteries and electronic devices must be disposed of in
accordance with the locally applicable regulations, not
with domestic waste.
11. Guarantee
This device is covered by a 3 year guarantee from the date of
purchase. The guarantee is valid only on presentation of the
guarantee card completed by the dealer (see back) confirming
date of purchase or the receipt.
• Batteriesandwearingpartsarenotincluded.
• Openingoralteringthedeviceinvalidatestheguarantee.
• Theguaranteedoesnotcoverdamagecausedbyimproper
handling, discharged batteries, accidents or non-compliance
with the operating instructions.
• Thecuffisincludedforthefunctionalguaranteeonly
(tightness) for 2 years.
Please contact aponorm
®
by microlife-Service (see foreword).
12. Technical Specifications
Operating temperature: 10 - 40 °C / 50 - 104 °F
15 - 95 % relative maximum humidity
Storage temperature: -20 - +55 °C / -4 - +131 °F
15 - 95 % relative maximum humidity
Weight: 340 g (including batteries)
Dimensions: 135,5 x 82 x 57 mm
Measuring procedure: oscillometric, corresponding to
Korotkoff method: Phase I systolic,
Phase V diastolic
Measurement range: 20 - 280 mmHg – blood pressure
40 - 200 beats per minute – pulse
Cuff pressure display 0 - 299 mmHg
range:
Resolution: 1 mmHg
Static accuracy: pressure within ± 3 mmHg
Pulse accuracy: ± 5 % of the readout value
Voltage source: • 4x1.5VBatteries;sizeAA
   • MainsadapterDC6V,600mA
(optional)
Reference to EN 1060-1 /-3 /-4; IEC 60601-1;
standards: IEC 60601-1-2 (EMC)
This device complies with the requirements of the Medical
Device Directive 93/42/EEC.
Technical alterations reserved.