Certification, Compliance and Labels
The manikin is CE marked in accordance with
Council Directive 1999/5/EC relating to Radio
and Telecommunications Terminal Equipment
(R&TTE), and Council Directive 2011/65/EU
on Restriction on the use of certain hazardous
substance (RoHS).
Australian Radiocommunications and EMC
Compliance Mark
CANADIAN ICES-003 STATEMENT
CAN ICES-3 (B)/NMB-3(B)
Manufacturer
Date of Manufacture
Dispose of in accordance with your country’s
recommendations.
Reference order number
Warning / Caution symbol
FCC Statement
This device complies with part 15 of the FCC rules.
Operation is subject to the following two conditions:
•
This device may not cause harmful interference
•
This device must accept any interference
received, including interference that may cause
undesired operation.
Caution
Changes or modifications not expressly approved by Laerdal Med-
ical could void the user’s authority to operate the equipment. This
equipment has been tested and found to comply with the limits
for a Class B digital device, pursuant to part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against
harmful interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause
harmful interference to radio communications. However, there is
no guarantee that interference will not occur in a particular instal-
lation. If this equipment does cause harmful interference to radio
or television reception, which can be determined by turning the
equipment off and on, the user is encouraged to try to correct
the interference by one or more of the following measures:
•
Reorient or relocate the receiving antenna.
•
Increase the separation between the equipment and receiver.
•
Connect the equipment into an outlet on a circuit different
from that to which the receiver is connected.
•
Consult the dealer or an experienced radio/TV technician
for help.
Contains FCC ID: U3O-G2M5477
Contains FCC ID: VVXLM400
Specifications
Resusci Anne QCPR, QCPR AED, QCPR D
Dimensions 69.7” x 20.5” x 9.8” (177 cm x 52 cm x 25 cm)
Weight: 79.2 lbs (36 kg)
Defibrillation Average of 2 x 360J/minute max (QCPR D only)
Operation temperature: 32°F to 104°F (0°C to +40°C)
Humidity: < 95% relative humidity
Storage temperature: 5°F to +122°F (-15°C to +50°C)
Ventilation
Supported airway management tools
The following intubation devices have been tested on the
Airway Head:
•
LMA Classic 4
•
LMA Classic 5
•
LMA Unique 5
•
LMA Fasttrack 4
•
LMA Fasttrack 5
•
Combitube 37 Fr
•
LTS-D 4
•
LTS-D 5
•
Japanese Sumi NA
Waste Handling
The manikin contains electronic components. Dispose of it at the
applicable recycling facility in accordance with local regulations.
European Directive 2012/19/EU (WEEE)
WEEE: this appliance is marked according to the European direc-
tive 2012/19/EU on Waste Electrical and Electronic Equipment
(WEEE). By ensuring this product is disposed of correctly, you
will help prevent potential negative consequences for the envi-
ronment and human health, which could otherwise be caused by
inappropriate waste handling of this product.
The symbol on the product, or on the documents accompanying
the product, indicates that this appliance may not be treated as
household waste. Instead it shall be handed over to the applica-
ble collection point for the recycling of electrial and electronic
equipment. Disposal must be carried out in accordance with
local environmental regulations for waste disposal. For more
detailed information about treatment, recovery and recycling of
this product, please contact your local city office, your household
waste disposal service or the Laerdal representative where you
purchased the product.
Warranty
The Laerdal Resusci Anne QCPR / QCPR AED / QCPR D has a
one-year limited Warranty. Refer to the Laerdal Global Warranty
for terms and conditions.
N25270
