Published
The present document contains requirements to demonstrate that Medical Body Area Network System (MBANS). The present document does not necessarily include all the requirements which may be required by a user, nor does it necessarily represent the optimum performance achievable. The types of devices that can belong to MBANSs are on-body and off-body medical sensors, patient monitoring devices and medical actuators covered by the Medical Device Directive (Directive 93/42/EEC [i.5]). The present document applies to the following MBANS applications which are considered to operate indoor:
• MBANS operating in the healthcare facility.
• MBANS operating in the patient's home.
NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.
Directive 2014/53/EU of The European Parliament and of the Council of 16 April 2014 on the harmonisation of the laws of the Member States relating to the making available on the market of radio equipment and repealing Directive 1999/5/EC
PUBLISHED
SRPS EN 303 203 V2.1.1:2016
60.60
Standard published
May 31, 2016