ENHANCED EXTERNAL COUNTERPULSATION TS4 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2005-11-01 for ENHANCED EXTERNAL COUNTERPULSATION TS4 * manufactured by Vasomedical, Inc..

Event Text Entries

[413500] Pt completed four treatments before returning to optometrist for a previously scheduled post-cataract evaluation. Hemorrhaging evident in both eyes, retinal artery aneurysm in right eye.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2435300-2005-00005
MDR Report Key644873
Report Source05,06
Date Received2005-11-01
Date of Report2005-10-31
Date of Event2005-09-26
Date Mfgr Received2005-09-30
Device Manufacturer Date2004-05-01
Date Added to Maude2005-11-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer Street180 LINDEN AVE.
Manufacturer CityWESTBURY NY 11590
Manufacturer CountryUS
Manufacturer Postal11590
Manufacturer Phone5169974600
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameENHANCED EXTERNAL COUNTERPULSATION
Generic NameDEVICE, EXTERNAL, COUNTER-PULSATING
Product CodeDRN
Date Received2005-11-01
Model NumberTS4
Catalog Number*
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key634361
ManufacturerVASOMEDICAL, INC.
Manufacturer Address* WESTBURY NY * US
Baseline Brand NameENHANCED EXTERNAL COUNTERPULSATION
Baseline Generic NameDEVICE, COUNTER-PULSATING, EXTERNAL
Baseline Model NoTS4
Baseline Catalog No*
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
10 2005-11-01

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