EMOTION Motion relax 600 User Manual - page 16
User manual relax 600 med/600
Version 1.0
Page 16 of 18
Only use original spare parts, therefore please contact us.
Warning: Retorque cranks and pedals
After the first 10 hours of use the cranks and pedals need to get re-tightened.
If they don´t get retightened, damage of the axle, pedals or cranks is possible and the warranty doesn´t cover
the damage.
5.3
Maintenance for authorised specialists
According to the transposition of the medical device directive 93/42 EEC into national law, emotion fitness calls
for a maintenance check with examination of all relevant component parts by an authorized employee/partner.
This maintenance check needs to be conducted every 12 months on all medical devices of emotion fitness. For all
necessitated control steps please also consider your countries local requirements.
5.4
Performance of the metrological control pursuant Medical Devices Operator Ordinance (not relevant for
units of the fitness line)
Medical products have to undergo a technical measurement check every 24 months. The date of the next
control is shown on the control badge, which you will find next to the type plate.
The possible calibration in the course of the technical measurement check can only get performed by an
authorised company or professional. Contact your dealer in case you need a reference.
5.5
Conduction of a safety-related control (According to the transposition of the medical device directive
93/42 EEC into national law)
At all medical training devices a technical safety check has to be conducted at least every 12 months and after
repair by an authorized employee or partner. This check needs to also include the control of the measurement
functionalities (speed and pulse) and all safety-relevant components.
The conduction of the Maintenance, Safety-Related Controls and Metrological Controls is in the sole
responsibility of the operator!
§ 2 subparagraph 2: This law also applies to the use, operation and maintaining of products that have not been
placed on the market as a medical device but are being used with the intended purpose of a medical device as
described in the national laws resulting from medical device directive 93/42EEC.
They are regarded as medical devices in terms of the medical device guideline.
6
Technical data
The information about measurements and weight can vary because of technical changes and optional
features
measurements
Weight
Max. user weight
159 cm x 65 cm x 137 cm (L/W/H)
82 kg
150 kg; boosted: 200 kg
System of resistance: self-powered brake without the external power supply
buffer battery: 3 x AA/ R03/ UM4 – mignon cell
range of performance medical: 15-500 watts/rpm dependent (25-1.000 watts/rpm independent)
range of performance fitness: 25-500 watts/rpm dependent (25-1.000 watts/rpm independent)
freewheel: existing
Following EU-guidelines are fulfilled:
DIN EN ISO 20957-1 SA
DIN EN ISO 20957-5 SA
DIN EN 60601-1
2001/95/EG general product safety guideline
93/42/EWG medical guideline (solely for medical units)