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Bionet Cardio7e - Safety Instructions for Electricity

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V 1.31
2021. 05 7 / 171 Doc. # : BN-OP-C7
Safety Instructions for Electricity
Please note the following precautions before using the product.
Is the power supply cord proper? (100 - 240V AC)
Is every cord connected properly to the product?
Is the grounding connected correctly? (Otherwise, noise can occur.)
There is a risk of electric shock if the Rest stand of the equipment is damaged or
can not be fixed to the product. Do not use the product and immediately ask
the manufacturer and the seller for repair
Classification.
This device is classified as follows, in accordance with IEC60601-1.
Its classification against electric shocks is Class , Type CF defibrillation -proof
applied part.
Degree of protection against harmful ingress of water: Ordinary
It is not proper to use this product near a flammable anesthetic or solvent.
Continuous operation.
IEC/EN60601-1-2 (Electromagnetic Compatibility Requirements) standard:
Classification
Description
Class A
The device or system is suitable for use in all establishments other than
domestic and those directly connected to the public low-voltage
power-supply network that supplies buildings used for domestic
purposes.
Mains power should be a typical commercial or hospital environment.
NOTE
Diagnosis provided by Cardio7e/Cardio7 must be confirmed by a qualified
medical professional.
NOTE
The EMISSIONS characteristics of this equipment make it suitable for use in industrial
areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which
CISPR 11 class B is normally required) this equipment might not offer adequate
protection to radio-frequency communication services. The user might need to take
mitigation measures, such as relocating or re-orienting the equipment.

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