Revision 15.00 / LB-0028
–
Cerebus Instructions for Use
24
Appendix 1
Warnings
1.
Only connect Cerebus System components to properly tested, grounded and dedicated AC
outlets using only the Blackrock provided power cable to reduce the risk of electrical shock.
Do not use an adapter for ungrounded wall outlets.
2.
Do not connect the Cerebus System to an outlet controlled by a wall switch.
3.
Do not use the Cerebus System in the presence of flammable anesthetic agents.
4.
Avoid strong static discharges from sources like televisions or computer monitors because
they can damage the electrical components of the system.
5.
Keep the Cerebus System away from liquids. Contact with water, shower spray, or wet
surfaces can lead to the patient receiving an electrical shock.
6.
Connection of external instruments may compromise electrical safety compliance with IEC
60601-1.
7.
The Cerebus System should be disconnected from any electrodes during cardiac
defibrillation.
8.
Place the Cerebus ® system in a secure location.
9.
Avoid tripping on cords connected to the Cerebus ® system.
Cautions
1.
Follow the restrictions of use for third party electrodes or arrays.
2.
Third party recording or control systems connecting to the Cerebus System and components
must be electrically isolated for subject safety.
Specifications
Model Name
Cerebus Neural Signal Processor
Power Requirements
110 (at 60 Hz) or 240 (at 50 Hz) VAC, 8.0
Amps maximum load
Serviceable Fuses
5 x 20mm, 250V, 1.6A, Slow Blow
Compliance Standards
IEC 60601-1, IEC 60601-1-2, IEC 60601-2-
26, CSA listed
Type of Protection
Class I (Amplifier Power Supply)
Degree of Protection
Type BF Applied Part (Neural Signal
Amplifier and Patient Cable Assembly)
Mode of Operation
Continuous
Water Ingress Protection
Ordinary Equipment, not fluid resistant,
IP20
Operating Environment
10˚C to 40˚C, 5 to 95% R.H. (non
-
condensing)
Storage Environment
-
20˚C to 50˚C, 5 to 100% R.H. (non
-
condensing)
