Ambu aScope Manuel d'utilisation - Page 8
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The Ambu® aScope™ Monitor function conforms with:
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Council Directive 93/42/EEC concerning Medical Devices.
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IEC 60601-1 Medical electrical equipment – Part 1: General requirements for basic safety and essential performance.
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EN 60601-1-1 Medical electrical equipment – Part 1-1 General requirements for safety – Collateral standard: Electromagnetic compatibility -
Requirements for test.
The Ambu® aScope™ power supply conforms with:
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Council Directive 93/42/EEC concerning Medical Devices.
-
IEC 60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance.
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EN 60601-1-1 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Electromagnetic compatibility -
Requirements for test.
7. Technical product specifications
Ambu® aScope™
Optical System
Field of View
Direction of View
Depth of Field
Illumination method
Insertion cord
Distal tip maximum temperature
(in ambient room temperature 23°C/73.4°F)
Bending section
Maximum width of inserted portion
Minimum ET-tube (inner diameter)
Working length
Scope
Total length
Luer channel (inner diameter)
Luer channel entry
Operating environment
Temperature
Relative humidity
Storage
Temperature
Relative humidity
Sterilisation
Method of sterilisation
Table 1 - Specification for the Ambu® aScope™
Ambu® aScope™ Monitor
Dimensions
Width
Height
Thickness
Weight
80°
0° (forward viewing)
2mm ~ 50 mm (0.1 – 1.968 inch)
LED (LTW-C282DS5-SE)
39°C (102.2°F)
Up 120°; down 120° (please be aware that the bending
section radius can be affected if the insertion cord is
not kept straight).
5.4mm (0.21")
6.0mm
630mm (24.8")
830mm (32.7")
0.8mm (0.03")
Luer connector
10 ~ 40°C (50 ~ 104°F)
30 ~ 85%
10 ~ 40°C (50 ~ 104°F)
30 ~ 85%
EO
196mm (7.76")
160mm (6.30")
142mm (5.60")
1150g (2.5lbs)
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