Guidance And Manufacturer's Declaration - Omron HEM-7530T-E3 Instruction Manual

16. Guidance and Manufacturer's Declaration

• This blood pressure monitor is designed according to the European Standard EN1060, Non-invasive sphygmomanometers
Part 1: General Requirements and Part 3: Supplementary requirements for electromechanical blood pressure measuring
systems.
• Hereby, OMRON HEALTHCARE Co., Ltd., declares that the radio equipment type HEM-7530T-E3 is in compliance with
Directive 2014/53/EU. The full text of the EU declaration of conformity is available at the following internet address:
www.omron-healthcare.com
• This OMRON product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., Japan.
• Please report to the manufacturer and the competent authority of the Member State in which you are established about any
serious incident that has occurred in relation to this device.
Applied part - Type BF, Type CF
Degree of protection against electric shock
,
(leakage current)
Ingress protection degree provided by
IP XX
IEC 60529
CE Marking
Temperature limitation
Symbols description
LOT number
Medical Device
Humidity limitation
Atmospheric pressure limitation
EN
EN59