Introduction; Intended Use - MIR Spirodoc User Manual

Keep the original packaging!
In the unlikely event that you have a problem with your device please use the original
packaging and return it to the distributor or manufacturer.
Should this be the case, please follow these guidelines:

Return the complete device in the original packaging.

Shipping costs any any customs duties must be paid by the sender.
Manufacturer‟s address:
MIR SRL
VIA DEL MAGGIOLINO, 125
00155 ROME (ITALY)
Tel ++ 39 0622754777
Fax ++ 39 0622754785
Web site: www.spirometry.com
Email: mir@spirometry.com
MIR has a policy of continuous product development and improvement. MIR
reserves the right to modify and update the information in this User's Manual
as deemed necessary. Any suggestions and or comments regarding this
product may be sent via email to: mir@spirometry.com.
MIR accepts no responsibility for any loss or damage caused by the user of
the device due to instructions contained in this Manual and/or due to
incorrect use of the product.
Please note that due to printing limitations, the screenshots shown in this
manual may differ from the display of the machine and/or from the keyboard
icons.
Copying this manual in whole or in part is strictly forbidden.
FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER
OF A PHYSICIAN
2.

INTRODUCTION

2.1

Intended use

The Spirodoc spirometer and pulse oximeter is intended to be used by a physician or
by a patient under the supervision/instruction of a physician or paramedic.
The lung function testing device is capable of performing:

spirometry testing in people of all ages, excluding infants and neonates

oximetry testing in people of all ages.
It can be used in any setting.
Spirodoc cod. 980156 Rev 1.3 EN 4/67