REFERENCE
TO STANDARDS
Device standard:
Device corresponds to the requirements of the European standard for non-inva-
sive blood- pressure monitor
IEC60601-1-6:2010+A1:2013/ EN60601-1-6:2010+A1:2015
IEC60601-1:2005+A1:2012/EN60601-1:2006+A11:2011+A1:2013+A12:2014
IEC60601-1-2:2014/ EN60601-1-2:2015
IEC/EN60601-1-11:2015
IEC80601-2-30:2009+A1:2013/EN80601-2-30:2010+A1:2015
Electrical compatibility:
Device fulfils the stipulations of the
The stipulations of the EU-Guidelines 93/42/EEC for Medical Products Class IIa
have been fulfilled.
TECHNICAL
SPECIFICATIONS
Measurement Procedure:
Display:
Measuring range:
Static press accuracy:
Measuring resolution:
Inflation:
Memory function:
Decompression:
Power source:
Rated voltage:
Operation temperature:
Operation humidity:
Storage temperature:
Cuff size:
Storage humidity:
Dimensions :
Oscillometric,
corresponding to Korotkoff method:
Phase I: systolic , Phase V: diastolic
Digital display
SYS/DIA
30 to 280 mmHg (in 1 mmHg increment)
Pulse: 40 to 200 beat/minute
±3mmHg
Pulse: ±5% of reading
1mmHg
Automatic inflation by internal pump
120 memory × 2 users(SYS, DIA, Pulse)
Constant exhaust valve system
2- size "AAA" alkaline Batteries
DC 3V 1.5W (direct current)
5~40°C/41~104°C
15%~85%RH maximum
-10~55°C/14~131°C
12.5- 21.5cm
10%~95%RH maximum
69 x 63 x29 ±1.0 mm
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