Important Patient and Safety Information
ST80i Stress Test System Instructions for Use xi
be determined by turning the device off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
– Reorient or relocate the receiving antenna
– Increase the separation between the device and receiver
– Connect the device into an outlet on a circuit different from that to which the
receiver is connected
– Consult the dealer or an experienced radio/television technician for help
The radio device used in this product is in compliance with the essential requirements and
other relevant provisions of Directive 1999/5/EC (Radio Equipment and
Telecommunications Terminal Equipment Directive). Class 1 radio equipment. Member
states may apply restrictions on putting this device into service or placing it on the market.
Industry Canada Statement:
This device complies with RSS-210 of the Industry Canada rules. Operation is subject to
the following two conditions:
– This device may not cause harmful interference, and
– This device must accept any interference received, including interference that may
cause undesired operation.
Ce dispositif est conforme à la norme CNR-210 d'Industrie Canada applicable aux
appareils radio exempts de licence. Son fonctionnement est sujet aux deux conditions
suivantes:
– Le dispositif ne doit pas produire de brouillage préjudiciable, et
– Ce dispositif doit accepter tout brouillage reçu, y compris un brouillage susceptible de
provoquer un fonctionnement indésirable.
This Class B digital apparatus complies with Canadian ICES-003.
Cet appareil numérique de la classe B est conforme à la norme NMB-003 du Canada.
The AIM’s LED blinks every two seconds when the AIM is functioning properly. If the
AIM LED does not blink, the AIM is not functioning properly.
The 5-pin connector port on the back of the AIM is non-functional.
Do not connect TC series cardiograph patient interface modules to the 5-pin connector
port on the back of the AIM.
Safety Information for the Wireless Patient Interface
Module
For information about electromagnetic compatibility (EMC) with surrounding devices, see
“Electromagnetic Compatibility (EMC) - To be finalized” on page E-7 of Appendix E,
“Specifications and Requirements”.
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