Ambu 620001000US Manuel d'utilisation - Page 7
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1.6. General notes
If, during the use of this device or as a result of its use, a serious incident has occurred,
please report it to the manufacturer and to your national authority.
2. System description
The aScope 5 Broncho must be connected to an Ambu displaying unit. For information about
Ambu displaying units, please refer to the respective displaying units' Instructions for use.
2.1. System parts
Ambu® aScope™ 5 Broncho
– Single-use device:
Product name
aScope 5 Broncho 2.7/1.2
aScope 5 Broncho 4.2/2.2
2.2. Product compatibility
The aScope 5 Broncho has been designed to be used in conjunction with:
Displaying units
– Ambu® aBox™ 2
– Ambu® aView™ 2 Advance
Note: Connector port colour and geometry on the displaying unit must match the connector colour and
geometry on the visualization device.
Endoscopic accessories
– Passive endotherapy instruments compatible with the working channel ID (such as biopsy
forceps, cytology brushes, endoscopic needles)
– Active endotherapy instruments compatible with the working channel ID (such as cryo probe)
– Accessories with standard Luer slip and/or Luer Lock (using the enclosed introducer)
aScope 5 Broncho 2.7/1.2 and 4.2/2.2 are not compatible with high frequency endotherapy instruments and laser.
*
Lubricants and solutions
– Sterile water
– Isotonic saline solution
– Waterbased lubricants
– Norepinephrine 0.5 mg
– Local anaesthetic gel and solutions e.g:
•
1 % lidocaine solution
•
2 % lidocaine gel
•
Lidocaine 10 % aerosol spray
Airway management accessories in compliance with EN ISO 5361
– Endotracheal tubes
– Laryngeal masks
– Tracheostomy tubes
Part numbers
624001000US aScope 5 Broncho 2.7/1.2
620001000US aScope 5 Broncho 4.2/2.2
60 cm/ 23.6"
Outer diameter [mm] "
2.7 mm/0.11"
max 3.2 mm/0.13"
4.2 mm/0.17"
max 4.8 mm/0.19"
Inner diameter [mm] "
1.2 mm/0.05"
2.2 mm/0.09"
*
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