Plusmed pM-B51 Mode D'emploi page 41

Note
This blood pressure monitor complies with the EC Directive (93/42/
EEC) and bears the CE mark This blood pressure monitor also com-
plies with mainly following standards (included but not limited):
Safety standard:
EN 60601-1 Medical electrical equipment part 1: General requirements
for safety
EMC standard:
EN 60601-1-2 Medical electrical equipment part 1-2: General requirements
for safety- Collateral standard: Electromagnetic compatibility- Require-
ments and tests
Performance standards:
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 non-invasive sphygmomanometers.
Follow instructions for use.
BF Classification:
• Internally powered equipment
• BF type applied part
• IPX0
• Not suitable for use in presence of flammable anesthetic mixture
with air or with Oxygen or nitrous oxide
• Continuous operation with short-time loading
Keep dry.
To avoid inaccurate results caused by electromagnetic interference bet-
ween electrical and electronic equipments, do not use the device near
a mobile phone or microwave oven. At least keep a maximum output
power of 2 W yields and a distance 3.3m away from this equipment.
Discard the used product to the recycling collection point according
to local regulations.