After Use - Ambu aScope 4 RhinoLaryngo Intervention Bedienungsanleitung

4.5. After use

Visual check 9
Inspect the endoscope for any evidence of damage on the bending section, lens, or insertion
cord. In case of corrective actions needed based on the inspection act according to local
hospital procedures.
Disconnect 10
Disconnect the endoscope from the Ambu displaying unit.
Disposal 11
Dispose of the endoscope, which is a single-use device . The endoscope is considered
contaminated after use and must be disposed of in accordance with local guidelines for
collection of infected medical devices with electronic components.
5. Technical product specifications
5.1. Standards applied
The endoscope function conforms with:
– EN 60601-1 Medical electrical equipment – Part 1: General requirements for basic safety and
essential performance.
– EN 60601-2-18 Medical electrical equipment – Part 2-18 Particular requirements for the basic
safety and essential performance of endoscopic equipment.
5.2. Endoscope specifications
Insertion cord
Bending section [°]
1
Insertion cord diameter [mm, (")]
Distal end diameter [mm, (")]
Maximum diameter of insertion portion [mm,
(")]
Minimum tracheostomy tube size (ID) [mm]
Working length [mm, (")]
Working channel
Minimum instrument channel width
Storage
Recommended storage temperature
Relative humidity [%]
Atmospheric pressure [kPa]
Optical system
Field of View [°]
Depth of Field [mm]
Illumination method
Suction connector
Connecting tube ID [mm]
Sterilisation
Method of sterilisation
aScope 4 RhinoLaryngo Intervention
130
5.0 (0.20)
5.4 (0.21)
5.5 (0.22)
6.0
350 (13.8)
aScope 4 RhinoLaryngo Intervention
[mm, (")] 2.0 (0.079)
2
aScope 4 RhinoLaryngo Intervention
[°C, (°F)] 10 ~ 25 (50 ~ 77)
3
30 ~ 85
80 ~ 109
aScope 4 RhinoLaryngo Intervention
85
6 - 50
LED
aScope 4 RhinoLaryngo Intervention
Ø6.5 - 9.5
aScope 4 RhinoLaryngo Intervention
ETO
,130