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