epistaxis, systemic infection, urinary tract infection, sedation induced apnea,
sedation induced CO
RF related: chest pain/discomfort, ventricular tachyarrhythmia, transient
•
ischemic attack (TIA), cerebrovascular accident (CVA), complete heart
block, coronary artery spasm, coronary artery thrombosis, coronary artery
dissection, cardiac thromboembolism, pericarditis, cardiac
perforation/tamponade, valvular damage and increased phosphokinase
level.
Unrelated to device or procedure: urinary retention, transient extremity
•
numbness, Parkinson's disease and gastrointestinal diverticulosis.
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THERE IS NO EXPRESS OR IMPLIED WARRANTY, INCLUDING WITHOUT
LIMITATION ANY IMPLIED WARRANTY OF MERCHANTABILITY OR
FITNESS FOR A PARTICULAR PURPOSE, ON THE PRODUCT(S)
DESCRIBED HEREIN. UNDER NO CIRCUMSTANCES SHALL
BIOSENSE WEBSTER, INC., OR ITS AFFILIATED COMPANIES, BE LIABLE
FOR ANY SPECIAL, DIRECT, INCIDENTAL, CONSEQUENTIAL, OR OTHER
DAMAGES OTHER THAN AS EXPRESSLY PROVIDED BY SPECIFIC LAW.
WITHOUT LIMITING THE FOREGOING, BIOSENSE WEBSTER, INC. OR ITS
AFFILIATED COMPANIES, SHALL NOT BE LIABLE FOR ANY SPECIAL,
DIRECT, INCIDENTAL, CONSEQUENTIAL, OR OTHER DAMAGES, ARISING
OUT OF THE REUSE OF ANY PRODUCT(S) LABELED FOR SINGLE USE
OR WHERE REUSE IS PROHIBITED BY APPLICABLE LAW.
Descriptions and specifications appearing in Biosense Webster, Inc. printed
matter, including this publication, are informational only and meant solely to
generally describe the product at the time of manufacture and are not made or
given as a warranty of the prescribed product in any way.
M-5276-785B
retention with lethargy and cholecystitis.
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