COMPLIANCE
Compliance with the European Directive 93/42/EEC for Medical Products
This device conforms to the following requirements: European Directive 93/42/EEC for Medical Products act; Medical Products Act; European Standards for Electrical Equipment EN
This is evidenced by the CE mark of conformity accompanied by the reference number of a designated authority.
This device was designed for use by adults only.
Compliance with the Australian EMC Frame Work
This device conforms to the following requirements: EMC Emission Standard for Industrial, Scientific and Medical Equipment AS/NZS
Environment for use
The device is for use in offices, sports facilities, and hospitals (waiting rooms), etc.
NOTE
This device does not have the function of automatic cycling measurement.
Therefore, a part of this device does not conform to
ii