DeVilbiss DV6 Series - Page 7

EN - 7A-DV6HH-HE
TABLE OF CONTENTS
Important Safeguards ................................................................................. EN - 7
Introduction ................................................................................................. EN - 7
Symbol Definitions ...................................................................................... EN - 7
Important Parts
Contents ................................................................................................. EN - 8
Understanding Your Device ................................................................... EN - 8
System Assembly ....................................................................................... EN - 9
Cleaning ..................................................................................................... EN - 10
Maintenance ............................................................................................... EN - 10
Sealing Gasket Placement ................................................................... EN - 10
Humidifier Water Chamber and Humidifier Cradle ................................ EN - 11
Expected Service Life ................................................................................. EN - 11
Product Disposal ........................................................................................ EN - 11
Troubleshooting .......................................................................................... EN - 11
Specifications ............................................................................................. EN - 11
Assembled in the USA
IMPORTANT SAFEGUARDS
• Refer to International Standard IEC 60601-1 Ed 3.0 Amendment 1 for safety
requirements applicable to Medical Electrical Systems.
• The height of the DV6 series device must be lower than the mask when using a
humidier to prevent water from getting into the mask.
• The humidier water chamber is intended for single-patient use only.
• Empty and dry humidier water chamber before transporting.
• Do not attempt to ll the water chamber while it is attached to the humidier
cradle. Damage to the humidier cradle may occur. Always remove the water
chamber from the humidier cradle before lling.
• Never touch the heater plate on the humidier cradle. Never touch the heat
transfer plate on the bottom of the water chamber. These plates can reach
temperatures as high as 149˚F (65˚C) during operation.
• Do not operate the heater if the water chamber is empty. The heater plate may
be turned off using CPAP Settings when device is being used without water.
INTRODUCTION
Indications For Use - Optional Heated
Humidifier
Use on the advice and prescription of a licensed physician to help relieve the
symptoms of dryness of the throat, nasal passages and the mouth, which are
common with positive airway pressure therapy. This is especially true in dry
climates and during the cold season when humidity in the air is typically lower
than at other times.
SYMBOL DEFINITIONS
Consult instructions for use RTCA / DO-160
Rx Only = Prescription required
C US
TUV Rheinland C-US
approval mark
Class II electrical protection-
double insulated
Catalog Number
Type BF equipment-applied part Serial Number
Manufacturer
EC REP
European Representative
Date of Manufacture
0044
European Rep CE mark
IP21
Ingress Protection - Protected against nger access to hazardous
parts; protected against vertically falling water drops
This device contains electrical and/or electronic equipment that must
be recycled per EU Directive 2012/19/EU-Waste Electrical & Electronic
Equipment