Operation Manual
Medical Test Supply    www.medicaltestsupply.com 
22
In addition, the overall check of the Sphygmomanometer, including the NIBP calibration 
and safety check such as the leakage current, should be only performed by qualified 
personnel once every 12 months. 
Warning
The disposal of scrap instrument  and its  accessories  and packing (including batteries, 
plastic bags, foams and paper boxes) should follow the local laws and regulations. 
EMC declaration: 
  When this device is installed or putted into service, EMC should be paid more attention, as 
the portable and mobile RF communications equipment with higher EM interference can affect 
this device. 
  The  internal  components  and  cables  should  not  be  changed,as  this  may  decreased 
IMMUNITY of the device. 
  The Electronic Sphygmomanometer should not be used adjacent to or stacked with other 
equipment. 
Classification: 
EMC: Group I Class B. 
According to the MDD 93/42, the classification of this medical device: a. 
The type of protection against electroshock: Class equipment. 
The degree of protection against electroshock: type BF applied part . 
The degree of protection against ingress of water: IPX0. 
According to the mode of operation: Continuous. 
According  to the  degree  of  safely  of application  in  the  presence  of  a  flammable  anesthetic 
mixture with air or with oxygen or nitrous oxide: Equipment not suitable for use in the presence 
of a flammable anesthetic mixture with air or with oxygen or nitrous oxide. 










