User's Manual

2120
SPECIFICATIONS
Power supply
3.7V 420mAH Built-in rechargeable lithium-ion
battery, 5V / 1A USB AC Adaptor
Display moder
Digital LCD V.A.46.5x36.5mm
Measurement mode
Oscillographic testing mode
Measurement range
Accuracy
Normal working condition
Storage & transportation
condition
Measurement perimeter
of the wrist
About 13.5cm-21.5cm
Net Weight
Approx.110g
External dimensions
Attachment
Approx.79.8×72.5×13.2mm
USB cable, AC Adaptor
user manual
Mode of operation
Continuous operation
Degree of protection
Type BF applied part
Protection against
ingress of water
IP22, It means the device could protected
against solid foreign objects of 12.5 mm and
greater, and against vertically falling water
drops when ENCLOSURE tilted up to 15°
Software version
Device classification
V01
Internally Powered ME Equipment
WARNING: No modification of this equipment is allowed.
Pressure: 0kpa-40kpa（0mmHg-300mmHg）
pulse value:(40-199)beat/minute
Pressure:
5℃-40℃within±0.4kpa(3mmHg)
0℃-45℃(out of 5℃-40℃)
within±0.7kpa(5mmHg)
pulse value:±5%
Temperature:-20℃ to 60℃ RH: 10% to 93%
Atmospheric pressure: 50kPa to 106kPa
Temperature:5℃ to 40℃ Relative humidity ≤85%
Atmospheric pressure: 86kPa to 106kPa
CONTACT INFORMATION
For more information about our products, please visit www.transtek.cn.you
can get customer service, usual problems and customer download, transtek
will serve you anytime.
Contact Information
Authorized European Representative:
Manufactured by:
GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD
Company:
GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD
Address:
Zone A, 5/F., Investment Building , No. 12, Huizhan East Rd., Torch
Development District, Zhongshan, Guangdong, 528437, China
Company:
MDSS - Medical Device Safety Service GmbH
Address:
Schiffgraben 41, 30175 Hannover, Germany
Complied European Standards List
EN 60601-1:2006/AC:2010
EN 60601-1-11:2010
EN 1060-1:1995+A2:2009
EN 1060-3:1997+A2:2009
EN 60601-1-2:2007/AC:2010
EN/ISO 14971:2007
EN/ISO 15223-1:2012
EN 1041:2008
Risk Management
Labeling
User Manual
General
Requirements
for Safety
Performance
Requirements
Electromagnetic
Compatibility
Clinical Investigation EN 1060-4:2004
Usability EN 60601-1-6 : 2010
EN 62366:2008
Software life-cycle
processes
EN 62304:2006/AC:2008
EN 80601-2-30:2010