AIROS 8 - Product Classification

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NOTE: This unit is not eld-serviceable. Tampering with or dismantling
this unit in any way will void warranty. If you have questions or need
assistance, please contact your local authorized dealer.
Manufactured for:
AIROS Medical, Inc.
2501 Monroe Blvd., Suite 1200
Audubon, PA 19403
1-866-991-6956
www.airosmedical.com
Product Classication
According to the type of protection against electrical shock, this device is classied
as a Class II Equipment, and Type BF Equipment that is powered by an external
electrical power source.
According to the degree of protection against harmful ingress of water this system
is classied as Ordinary Equipment (IPx0: without protection against ingress of
water)
According to the degree of protection against harmful ingress of water, this system
is classied as Ordinary Equipment (IP21: Protected against solid foreign objects of
12.5mm Ø and greater. Protection against vertically falling water drops.)
This system is classied as Equipment not suitable for use in the presence of a
ammable anesthetic mixture with air or oxygen or nitrous oxide.
According to the mode of operation this system is classied as Equipment that can
be used for Continuous Operation.
NOTE: In the USA, Federal Law restricts this device to sale, by or on
the order of a physician.
NOTE: Unit is packaged for transportation by common carrier. The
device must be operated by qualied and trained personnel only.
NOTE: Do not position the device in a way that makes it difcult to
unplug the power plug. Modication of this equipment is not allowed.