Technical Specifications; Environmental Conditions - Anspach eMax 2 Manual De Instrucciones

English

Technical Specifications

The device complies with the following standards:
IEC 60601-1:2005: + CORR. 1 (2006) + CORR. 2 (2007), EN 60601-1:2006 +A11:2011, ANSI/AAMI ES60601-1:2005, CAN/
CSA-C22.2 No.60601-1:08, (3rd edition) Medical electrical equipment part 1: General requirements for basic safety and
essential performance;
UL 60601-1:2003 (Revised 2006), IEC 601-1:1988 +A1:1991 + A2:1995; EN60601-1:1990 with A1 and A12:1993,
A2:1995 and A13:1996; and CAN/CSA C22.2 No. 601.1-M90, Standard for Medical Electrical Equipment – Part 1 General
Requirements for Safety
With regard to electrical shock, fire, mechanical hazards, this ETL classified device conforms to AAMI STD ES60601-1, UL
STD 60601-1, and is certified to CSA STD C22.2 No.60601-1 and 601.1
This device complies with applicable EEC directives. Medical Device Directive 93/42/EEC as amended by 2007/47/EC.
Machinery Directive 2006/46/EC.
Temperature
Relative Humidity
Atmospheric
Pressure
Primary: 100-240VAC, 50/60 Hz, 250 VA
Class I: Protective Earth
Fluid Ingress Protection: IPX0
Type B: Applied Part, Continuous Operation
Size: 26.7 cm x 16.5 cm x 14.7 cm (10.5 in x 6.5 in x 8.5 in)
Weight: 2.0 kg (4.41 lbs)
Cord: 3.66 m (12 ft) in length
Fluid Ingress Protection: IPX8
10

Environmental Conditions

Operating: 18°-30°C (65°-85°F)
Transportation and Storage: -29° – +50°C (-20° - +120°F)
Operating: 30% to 70%
Transportation and Storage: 10% to 90%
Operating: 0.7–1.06bar
Transportation and Storage: Not applicable
Console (SC2100, SC2101, and SC2102) Specifications
Foot Pedal (E-FP, E-FP-DIR, E-FP-DIR/IRR) Specifications