AEG BMG 5612 520612 Manual Do Utilizador
Códigos do produto
520612
English
82
CONTRAINDICATION
It is inappropriate for people with serious arrhythmia to use this Electronic Sphyg-
momanometer.
momanometer.
PRODUCT DESCRIPTION
Based on Oscillometric methodology and silicon integrated pressure sensor, blood pres-
sure and pulse rate can be measured automatically and non-invasively. The LCD display
will show blood pressure and pulse rate. The most recent 3x40 measurements can be
stored in the memory with date and time stamp. The monitor can also show the average
reading of the last three measurements.
The Electronic Sphygmomanometers corresponds to the below standards: IEC 60601-
1:2005/EN 60601-1:2006/AC:2010 (Medical electrical equipment -- Part 1: General require-
ments for basic safety and essential performance), IEC60601-1-2:2007/EN 60601-1-2:2007
/AC:2010 (Medical electrical equipment -- Part 1-2: General requirements for basic safety
and essential performance - Collateral standard: Electromagnetic compatibility - Require-
ments and tests), IEC 80601-2-30:2009+Cor.2010/EN 80601-2-30:2010(Medical electrical
equipment –Part 2-30: Particular requirements for the basic safety and essential perfor-
mance of automated non-invasive sphygmomanometers) EN 1060-1: 1995 + A1: 2002 +
A2: 2009 (Non-invasive sphygmomanometers - Part 1: General requirements), EN 1060-3:
1997 + A1: 2005 + A2: 2009 (Non-invasive sphygmomanometers - Part 3: Supplementary
requirements for electro-mechanical blood pressure measuring systems), ANSI/AAMI SP-
10:2002+A1:2003+A:2006.
sure and pulse rate can be measured automatically and non-invasively. The LCD display
will show blood pressure and pulse rate. The most recent 3x40 measurements can be
stored in the memory with date and time stamp. The monitor can also show the average
reading of the last three measurements.
The Electronic Sphygmomanometers corresponds to the below standards: IEC 60601-
1:2005/EN 60601-1:2006/AC:2010 (Medical electrical equipment -- Part 1: General require-
ments for basic safety and essential performance), IEC60601-1-2:2007/EN 60601-1-2:2007
/AC:2010 (Medical electrical equipment -- Part 1-2: General requirements for basic safety
and essential performance - Collateral standard: Electromagnetic compatibility - Require-
ments and tests), IEC 80601-2-30:2009+Cor.2010/EN 80601-2-30:2010(Medical electrical
equipment –Part 2-30: Particular requirements for the basic safety and essential perfor-
mance of automated non-invasive sphygmomanometers) EN 1060-1: 1995 + A1: 2002 +
A2: 2009 (Non-invasive sphygmomanometers - Part 1: General requirements), EN 1060-3:
1997 + A1: 2005 + A2: 2009 (Non-invasive sphygmomanometers - Part 3: Supplementary
requirements for electro-mechanical blood pressure measuring systems), ANSI/AAMI SP-
10:2002+A1:2003+A:2006.
SPECIFICATIONS
1. Product name: Blood Pressure Monitor
2. Model: BMG 5612 (BM-091)
3. Classification: Internally powered, Type BF applied part, IPX0, No AP or APG, Continu-
2. Model: BMG 5612 (BM-091)
3. Classification: Internally powered, Type BF applied part, IPX0, No AP or APG, Continu-
ous operation
4. Device size: Ca 104 mm x 45 mm x 154 mm
5. Cuff circumference: 22 cm-30 cm (Optional), 30 cm-42 cm, 42 cm-48 cm (Optional)
6. Weight: Approx 269 g (batteries and cuff excluded)
7. Measuring method: Oscillometric method, automatic inflation and measurement
8. Memory volume: 3 x 40 measurements with time and date stamp
9. Power source: Batteries: 4 x 1.5 V type AA • Mignon • LR6
5. Cuff circumference: 22 cm-30 cm (Optional), 30 cm-42 cm, 42 cm-48 cm (Optional)
6. Weight: Approx 269 g (batteries and cuff excluded)
7. Measuring method: Oscillometric method, automatic inflation and measurement
8. Memory volume: 3 x 40 measurements with time and date stamp
9. Power source: Batteries: 4 x 1.5 V type AA • Mignon • LR6
Power supply: DC 6 V, 600 mA