2
EN
Product information
This product information may be updated without further notice. Copies of the current version are available from
the manufacturer.
Contents
Page
1. Warnings/Cautions
3
2. Introduction
4
2.1. Intended
use
4
2.2. Contraindications
4
3. Specifi
cations
4
3.1. Materials
5
4.
Principles of operation
6
5. Adverse
effects
6
6.
Preparation for use
6
6.1. Functional
testing
6
6.1.1.
Test 1 - Visual inspection
7
6.1.2.
Test 2 - Infl ation/defl ation test
7
7. Insertion
8
7.1. Pre-insertion
preparation
8
7.2. Insertion
8
7.3. Insertion
techniques
8
7.3.1. Placement
technique
9
7.4. Insertion
problems
9
7.5. Infl
ation
9
7.6.
Connecting to the anesthetic system
10
7.7. Fixation
10
7.8.
Usage with spontaneous ventilation
11
7.9.
Usage with positive pressure ventilation
11
7.10.
Critical observations during use
11
7.11. Recovery
12
7.12. Removal
procedure
12
8. Specialized
use
12
8.1.
Intubation through the Ambu AuraOnce
12
8.2.
Use of the Ambu AuraOnce for blind tracheal intubation
13
8.3. Pediatric
Use
13
8.4.
Critical situations and emergencies
13
8.4.1. Critical
situations
13
8.4.2. Emergencies
13
8.5.
Magnetic resonance imaging (MRI)
13
Illustration
14-15
Symbols
16
Addresses
17
US: Rx only
Ambu
®
is registered trademark of Ambu A/S, Denmark.
Ambu A/S is certifi ed according to ISO 9001, and ISO 13485.
