DMG MixStar eMotion Instrucciones De Uso página 87

MixStar eMotion
Packaging
Starter Pack
1 MixStar eMotion 230 V International
1 MixStar eMotion 115 V Int. International
1 MixStar eMotion 115 V USA
1 MixStar eMotion 230 V GB
1 MixStar eMotion 230 V NZ/AUS
Accessories
1 Foot Switch
50 MixStar Tips
50 MixStar Tips Honigum Pro
Medical Device
en-us Medical Device
de Medizinprodukt
fr Dispositif médical
it Dispositivo medico
es Producto sanitario
pt-br Dispositivo médico
nl Medisch hulpmiddel
da Medicinsk udstyr
sv Medicinteknisk produkt
This equipment has been tested and found to comply with the limits
for a Class A digital device, pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against
harmful interference when the equipment is operated in a commercial
environment. This equipment generates, uses, and can radiate radio
frequency energy and, if not installed and used in accordance with the
instruction manual, may cause harmful interference in which case the
user will be required to correct the interference at his own expense.
Caution: Changes or modifications not expressly approved by the party
responsible for compliance could void the user´s authority to operate
the equipment.
Service Address USA:
DMG America
65 Challenger Road, Suite 340 Ridgefield Park, NJ 07660 | USA
Federal Law (USA) restricts this device to sale by or on order of a dentist
or other practitioner licensed by law of the state in which he or she
practices to use or order the use of this device.
REF 900480
REF 900482
REF 999482
REF 900483
REF 900484
REF 900310
REF 909567
REF 903334
pl Wyrób medyczny
ru Медицинское изделие
tr Tıbbi cihaz
ro Dispozitiv medical
cs Zdravotnický prostředek
el Іατροτεχνολογικό προϊόν
zh 医疗器械
ja 医療機器
ko 의료 기기
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