p/n 18603-001, Rev. C LTV
®
1200/1150 Ventilator Service Manual Page iii
Notices
The LTV
®
1200/1150 ventilator complies with limitations as specified in IEC 601-1-2 for
Medical Products. It does however, use and radiate radio frequency energy.
The function of this machine may be adversely affected by the operation of other nearby
equipment, such as high frequency surgical diathermy equipment, short-wave therapy
equipment, defibrillators or MRI equipment.
European Regulatory Requirements per 93/42/EEC Medical Device Directives
Pulmonetic Systems European Representative for vigilance reporting within the European Community
is:
MediMark® Europe Sarl.
11, rue Emile Zola. BP 2332
F-38033 Grenoble Cedex 2. France
Tel: +33 (0)4 76 86 43 22
Fax: +33 (0)4 76 17 19 82
E-mail: info@medimark-europe.com
Any product malfunctioning issues that fall under Medical Device Directives Essential Requirements
should be directed to MediMark.
Notice to Users
Unsafe Operation - Servicing the LTV
®
1200/1150 ventilator without a complete and
thorough understanding of its attributes may result in unsafe operating conditions. It is
important that this manual be read and understood in its entirety before servicing the
ventilator.
Warnings and Cautions Section - Read the section on Warnings and Cautions carefully
before attempting to service or operate the LTV
®
1200/1150 ventilator. General warnings
and cautions which apply any time you use the ventilator are listed in the front of this
manual. General and specific warnings and cautions also appear throughout the text where
they are most meaningful.
Use and Maintenance - Any questions regarding installing, setting up, operating, or
maintaining the LTV
®
1200/1150 ventilator, should be directed to a service technician who
has been trained and certified by Pulmonetic Systems to service the LTV
®
1200/1150
ventilator or Pulmonetic Systems using the contact information at the front of this manual.
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