Edwards Vigilance Ii Service Manual

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  2. Edwards Vigilance Ii Service Manual 2018
  1. Edwards Vigilance 8 0 - IB-ED701-A.0 #701 0844 Edwards Vigilance II 8 0 - IB-ED702-A.0 #702 0844 Edwards Vigileo 8 0 - IB-ED703-A.0 #703 0844 Gambro Prismaflex 8 0 - IB-ED803-A.0 #803 1020 IntelliVue TcG10 2 0 - IB-ED301-A.0 #301 1020 up to 1 up to 1 External device connected using VueLink up to 6c up to 2c - n/a up to 2 up to 4.
  2. View online Quick reference manual for Edwards Vigilance II Medical Equipment or simply click Download button to examine the Edwards Vigilance II guidelines offline on your desktop or laptop computer.
  3. Since the introduction of the Swan-Ganz catheter in the early 1970s, Edwards Lifesciences has partnered with clini- cians to develop products and systems that advance the care and treatment of the critically ill.
Edwards vigilance ii service manual

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EDWARDS LIFESCIENCES, PR SWAN-GANZ CCOMBO V CCO/SVO2/CEDV/VIP THERMODILUTION CATHETER AMC THROMBOSHIELD SWAN-GANZ CATHETERBack to Search Results
Model Number 777HF8J
Device Problem Incorrect, Inadequate or Imprecise Resultor Readings (1535)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 02/28/2012
Event Type Malfunction
Event Description

It was reported that 'unstable cco value was observed during use. It is unknown what the readings were or if there were any error messages observed. There was no damage noted on the catheter. ' the sample of tracing was not available. There were no patient complications reported.

Manufacturer Narrative

One catheter was returned with monoject 1. 5cc limited volume syringe for evaluation. No introducer or contamination shield was returned. The thermistor read 37. 0 c when submerged into a 37. 0 c water bath. The catheter was connected to the vigilance i monitor and vigilance ii monitor and 'check thermal filament position' error message was shown on both monitors. According to the operator's manual for the vigilance ii monitor, possible causes for the 'check thermal filament position' message are the following: 'flow around thermal filament may be reduced. Thermal filament may be against vessel wall. Catheter not in patient. ' these error messages can be expected during testing in a static water bath. Thermistor and thermal filament circuit were continuous; there were no open or intermittent conditions. No visible inconsistencies were observed on eeprom data. Both thermistor and thermal filament connectors were opened and found no visible inconsistencies. Resistance value of the thermal filament circuit was measured at 37. 66 ohms, which is within specifications. All through lumens were patent without leakage or occlusion. The balloon inflated clear, concentric and remained inflated for more than 5 minutes without leakage. No visible damage to the catheter body or returned syringe was observed. The lot number was not provided; therefore, a review of the manufacturing records could not be completed. Visual examinations were performed under 10x magnification. This type of report has been confirmed as related to the manufacturing process. An investigation is underway to determine what actions are needed to prevent recurrence of this type of complaint.

Manufacturer Narrative

At the initial investigation of the complaint, this was considered an isolated event. A deeper investigation identified a larger issue and corrective actions were implemented. In addition, an awareness training was given to the manufacturing personnel.

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Edwards Vigilance Ii Service Manual Online

Edwards Vigilance Ii Service Manual

Edwards Vigilance Ii Service Manual 2018

Type of DeviceSWAN-GANZ CATHETER
Manufacturer (Section D)
EDWARDS LIFESCIENCES, PR
state rd indus pk 402 km 1.4
anasco PR 00610
Manufacturer (Section G)
EDWARDS LIFESCIENCES, PR
state rd indus pk 402 km 1.4
anasco PR 92614
Manufacturer Contact
frances preston
one edwards way
irvine, CA 92614
9492505190
MDR Report Key2508170
MDR Text Key2577768
Report Number2015691-2012-17178
Device Sequence Number1
Product Code DQE
Combination Product (Y/N)N
Reporter Country CodeJA
PMA/PMN NumberK040287
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source TypeForeign,Health Professional,User facility,Company Representative
Reporter Occupation
Type of ReportInitial,Followup
Report Date02/28/2012
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received03/28/2012
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device MODEL Number777HF8J
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? No
Was the Report Sent to FDA? No
Distributor Facility Aware Date02/28/2012
Event Location Hospital
Date Manufacturer Received02/28/2012
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial