Pediatric Energy Reducer: Energy Attenuation Factor
50%
25%
20%
15%
7.4
Battery
Category
Part No
Non-rechargeable
Capacity
Shelf Life
Battery capacity measured according to IEC 60601-2-4, clause 102.3.2 at room tempe-
rature. Capacity may be diminished at operating temperature extremes, or when the
available battery charge is used in multiple power ON/OFF cycles.
7.5
Electrodes
Do not use defibrillation pads not approved by M&B. Use of unauthorized defibrillation
pads may cause the device to operate improperly and provide false measurements.
Follow all labeling instructions on the defibrillation pads
7.6
Guidance and manufacturer's declaration
7.6.1
Electromagnetic emissions (IEC 60601-1-2 Table 201)
The AED7000 is intended for use in the electromagnetic environment specified below. The customer
or the user of the AED7000 should assure that it is used in such an environment.
Emissions test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions IEC
61000-3-2
Voltage fluctuations/ flicker
emissions IEC 61000-3-3
Medical Electrical Equipment requires special precautions regarding EMC and must be installed and
put into service according to EMC information provided in this document.
30
25 Ω
50Ω and 75Ω
100Ω and 125Ω
150Ω and 175Ω
Compliance
Group 1
Class B
Not applicable
Not applicable
Specification
CR123A-4x2
12V d.c. 2.8Ah
100 discharges at 200J or 120 discharges at 150J
5 years (25°C ± 15°C)
Electromagnetic environment
guidance
TheAED7000 uses RF energy only for
its internal function. Therefore, its RF
emissions are very low and are not likely
to cause any interference in nearby
electronic equipment.