User Manual: HotDog
TM
Patient Warming System Controller
Page 19
Power Cord
4.6 m (15 ft) - May vary by country and region per local requirements and
regulations.
Device Ratings
Input: 100-240 VAC, 50/60 Hz, 850VA
Output A & B: 48 VDC, 480 VA Max each
Output C: 240 VA Max
Output D & E: 48 VDC, 144 VA Max each
Fuses
T10AL250V (2 x 5x20mm)
Environmental Conditions
Environmental Conditions for Transport
and Storage
Temperature: -20°C to 60°C
Humidity: 20% to 80%
Keep Dry
Environmental Conditions for Use
Temperature: 15°C to 25°C
Humidity: 20% to 80%
Classification and Standards
Certifications
IEC 60601-1; EN 60601-1-2; UL 60601-1; CAN/CSA-C22.2, No. 601.1, EN 55011
Classification
Classified under IEC 60601-1 Guidelines (and other national versions of the
Guidelines) as Class I, Type BF, Ordinary equipment, Continuous operation. Not
suitable for use in presence of flammable anesthetic mixtures with air or with
oxygen or nitrous oxide. Classified by Intertek Testing Services NA Inc. with
respect to electric shock, fire, and mechanical hazards only, in accordance with
UL 60601-1. Classified under the Medical Device Directive (93/42/EEC) as a Class
IIb device. Classified under the Canadian Medical Device Regulation as Class II.
Diagnostics
A qualified technician can perform general system testing. The Controller has no
user serviceable parts.
Important Information
This device complies with the EMC requirements according to IEC 60601-1-2.
Radio transmitting equipment, cellular phones, etc. shall not be used in the
close proximity of the device since this could influence the performances of the
device. Particular precaution must be considered during use of strong emission
sources such as High Frequency surgical equipment and similar so that, e.g., the
HF-cables are not routed on or near the device. If in doubt, contact a qualified
technician or your local representative.
