Pentax EPK-i7010 Instructions For Use Manual page 8

1-8. MAINTENANCE
1. Periodically this equipment and any applicable accessories should be inspected for operation and safety.
1-9. DISPOSAL
1. The equipment should be returned for disposal to PENTAX Medical.
Contact your local PENTAX Medical representative or service facility.
1
An information on Disposal for users in the European Union
This product is a medical device. In accordance with European Directive 2002/96/EC on Waste Electrical and
Electronic Equipment, this symbol indicates that the product must not be disposed of as unsorted waste, but
should be collected separately. Contact your local PENTAX Medical service facility for correct disposal and
recycling.
By disposing of this product correctly you will help ensure that the waste undergoes the necessary treatment,
recovery and recycling and thus prevent potential negative effects on the environment and human health which
could otherwise arise due to inappropriate waste handling.
POWER REQUIREMENTS
Check the standard power plug configurations that are used in your country. If the appropriate power cord is not
included in your product, notify your local PENTAX Medical service facility.
SOFTWARE VERSION
The software version of the products corresponding to this IFU is described on its back cover.
SYMBOLS ON MARKING
SYMBOLES DISTINCTIFS
Manufacturer
Fabricant
Date of manufacture
Date de fabrication
Alternating current
Courant alternatif
Type BF applied part (Safety degree specified by IEC 60601-1)
Partie appliquée de type BF (niveau de sécurité spécifié par la norme CEI 60601-1)
Switches the power on and off.
Mise sous/hors tension
Warning
Avertissement
Warning, electricity
Avertissement, électricité
Caution
Attention
Warning; Hot surface
Avertissement : surface chaude
3
Safety Precautions - Important