Operator’s Manual LTV
®
Series ventilator Page iii
p/n 10664, Rev. Y
Notices
The LTV
®
Series 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.
The LTV Series ventilator may emit and receive electromagnetic interference. Avoidance of this
exposure is recommended whenever possible.
Federal law restricts this device to sale by or on the order of a physician.
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.
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