Specifications Specifications
International Standards:
AAMI / ANSI SP10:2002/(R) 2008 & 2002/A1:2003/(R) 2008 &
2002/A2:2006/(R)2008
Manual, electronic, or automated sphygmomanometers
European Directive 93/42 EEC for Medical Products Act EN 60601-1
Medical electrical equipment part 1: General requirements for safety
EN 60601-1-2 Medical electrical equipment part 1-2: General
requirements for safety- Collateral standard: Electromagnetic
compatibility-
Requirements and tests
EN 1060-1 Non-invasive sphygmomanometers - General
requirements
EN 1060-3 Non-invasive sphygmomanometers - Supplementary
requirements for electromechanical blood pressure measuring systems.
EN 1060-4 Non-invasive sphygmomanometers - Test procedures to
determine the overall system accuracy of automated noninvasive
sphygmomanometers.
Specifications are subject to change without notice.
Specifications Warranty
Correct Disposal of This Product
(Waste Electrical & Electronic Equipment)
This marking shown on the product indicates that it should not
be disposed with other household waste at the end of its life.
To prevent potential harm to the environment or to human health,
please separate this product from other types of wastes and
recycle it responsibly. When disposing this type of product,
contact the retailer where product was purchased or contact your
local government office for details regarding how this item can
be disposed in an environmentally safe recycling center.
Business users should contact their supplier and check the terms
and conditions of the purchasing agreement. This product should
not be mixed with other commercial wastes for disposal. This
product is free of hazardous materials.
The Blood Pressure Monitor has been carefully manufactured
and inspected and is warranted to be free from defectives in
workmanship and materials. Under this warranty, Drive Medical’s
obligation shall be limited to the replacement of any such units
which prove, by Drive Medical’s inspection, to be defective within
two years from the original purchase date. If you have to send in
the unit enclose a copy of your receipt and clearly state the defect.
This warranty is not transferrable or assignable to any subsequent
purchaser or owner. Any abuse, operation other than the intended
use of this product as outlined in the manual, negligence, accident,
or repairs by someone, shall immediately void this warranty.
The foregoing warranty is exclusive and in lieu of all other
expressed warranties. Implied warranties, if any, including but not
limited to the implied warranties of merchantability and fitness for
a particular purpose, shall not extend beyond the duration of the
express warranty provided herein. In no event shall Drive Medical or
its subsidiaries by liable for loss of use or profit or other collateral,
special or consequential damages.
Cuff Circumference
Approx. 75 (W) × 300 (L) mm
Fits wrist circumference 13.5 - 21.5 cm (5.3” - 8.5”)
Operating Environment
Temperature 10ºC~ 40ºC (50°F ~104°F)
Humidity 15% ~90%RH
Pressure Atmospheric Pressure
Storage Environment
Temperature -20ºC~ 55ºC (-4°F ~131°F)
Humidity 15% ~90%RH
Classification
Internal Powered Equipment,Type BF
, Cuff is the Applied Part
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