Cleaning Instructions; Storage; Proper Use And Maintenance; Diagnostics - 3M Bair Hugger 875 Manuel De L'utilisateur

Cleaning Instructions

1. Disconnect the patient adjustable warming unit from the power
source before cleaning.
2. Cleaning should be performed in accordance with hospital
practices for cleaning or equipment. After every use; wipe
the warming unit, the outside of the warming unit hose, and
any other surfaces that may have been touched. Use a damp,
soft cloth and a hospital approved mild detergent, germicidal
disposable wipes, disinfecting towelettes, or antimicrobial
spray.
The following active ingredients are acceptable for use in cleaning
the warming unit:
• Oxidizers (e.g. 10% Bleach)
• Quaternary Ammonium Compounds (e.g. 3M™ Quat
Disinfectant Cleaner)
• Phenolics (e.g. 3M™ Phenolic Disinfectant Cleaner)
3. Let air dry.
Notice:
• Do not use cleaning solutions with greater than 80% alcohol
or solvents, including acetone and thinner, to clean the patient
adjustable warming unit or hose. Solvents may damage the
labels and other plastic parts.
• Do not immerse the Bair Hugger patient adjustable warming
unit, patient adjustable warming unit parts, or accessories in
any liquid or subject them to any sterilization process.

Storage

Store all components in a cool, dry place when not in use.

Proper Use and Maintenance

3M assumes no responsibility for the reliability, performance, or
safety of the patient adjustable warming unit if:
• Modifications or repairs are performed by unqualified
personnel,
• The patient adjustable warming patient adjustable warming unit
is used in a manner other than that described in the Operator's
Manual, or the Preventive Maintenance Manual
• The patient adjustable warming patient adjustable warming
unit is installed in an environment that does not meet the
appropriate electrical and grounding requirements.
• The warming unit not maintained in accordance with the
procedures described in the Preventive Maintenance Manual.

Diagnostics

A qualified service technician can perform over-temperature
detection system testing, temperature output testing, operating
temperature calibration, and error/fault code troubleshooting.

Read Before Servicing Patient Adjustable Warming Unit

All repair, calibration, and servicing of the Model 875 patient
adjustable warming unit must be performed by qualified, medical
equipment service technicians who are familiar with good practice for
medical device repair. If the patient adjustable warming unit does not
require the manufacturer's attention, we will ship replacement parts
to your location. Perform all repairs and maintenance in accordance
with the instructions provided with the replacement parts.

Technical Support and Customer Service

USA

TEL: 800-733-7775

OUTSIDE OF THE USA

Contact your local 3M Patient Warming representative.
8

When You Call for Technical Support

Please be ready to give the technical support representative the
serial number of your Bair Hugger patient adjustable warming unit.
The serial number is located on the back of the patient adjustable
warming unit.

Repair and Exchange

Call 3M if your Model 875 patient adjustable warming unit requires
service. A customer service representative will give you a Return
Authorization (RA) number. Please use this RA number on all
correspondence concerning your patient adjustable warming unit.
Your customer service representative will also send a shipping carton
to you at no charge upon request.
Please report a serious incident occurring in relation to the device
to 3M and the local competent authority (EU) or local regulatory
authority

Symbol Glossary

Symbol Title Symbol
Manufacturer
Authorized
Representative
in European
Community
Date of
Manufacture
Catalogue number
Serial number
Keep dry
Consult instructions
for use
Caution
Medical Device
3M™Bair Hugger™ Patient Adjustable Warming Unit Model 875 Operator's Manual
Description and
Reference
Indicates the medical
device manufacturer.
Source: ISO 15223, 5.1.1
Indicates the authorized
representative in the
European Community.
Source: ISO 15223, 5.1.2,
2014/35/EU, and/or
2014/30/EU
Indicates the date when
the medical device was
manufactured. Source:
ISO 15223, 5.1.3
Indicates the manufacturer's
catalogue number so that
the medical device can
be identified. Source :
ISO 15223, 5.1.6
Indicates the manufacturer's
serial number so that a
specific medical device
can be identified. Source:
ISO 15223, 5.1 .7
Indicates a medical device
that needs to be protected
from moisture. Source:
ISO 15223, 5.3.4
Indicates the need for
the user to consult the
instructions for use. Source:
ISO 15223, 5.4.3
Indicates the need for
the user to consult the
instructions for use for
important cautionary
information such as
warnings and precautions
that cannot, for a variety of
reasons, be presented on
the medical device itself.
Source: ISO 15223, 5.4.4
Indicates the item is a
medical device.