User and Technical Manual: HotDog Temperature Management Controller
Page 21
point + 3°C. (46°C) Medium Priority Alarm sounds.
Port M (Warming Mattress)
Independent electronic circuit shuts the heater off if the Warming Mattress temperature sensor reaches max set
point ± 2.5°C (42.5°C) Medium Priority Alarm sounds.
Over-current limits
Port A
10 amps max
Port B
10 amps max
Port C
10 amps max
Port D
10 amps max
Port M
7 amps max
Port T
Trucore
1 amp max
System
14.6 amps
Medium Priority Alarm sounds in over current condition. System utilizes power rationing when multiple ports are
drawing current over system levels.
System Over-current Protection
Dual input fused lines. Medium Priority Alarm sounds
Electrical Characteristics
Leakage Current
Meets UL 60601-1 and IEC 60601-1 requirements for Class I, Type BF equipment.
Power Consumption
850W maximum
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, C, D: 48 VDC, 480 VA Max each
Output M: 336 VA Max
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%
Technical Description of PCLCS (physiologic closed-loop control system)
–
AUTO mode -- per IEC 60601-1-10 ed. 1.1
Accompanying Information
From Table C.3
Details necessary for the safe use
of a
DISTRIBUTED PCLCS
6.4
NA - Not a distributed PCLCS
Summary of the
PCLC
modes of
operation and specification of
PCLCS
responses 8.2.2.6
See Table 2 in IFU
Means to check responses of the
PCLCS
8.2.2.6
If patient temperature is outside a normal range, AUTO mode is
disengaged and E7 alert is initiated.
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
