GELSOFT ERS 691008B

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-06 for GELSOFT ERS 691008B manufactured by Vascutek Ltd..

MAUDE Entry Details

Report Number9612515-2020-00001
MDR Report Key9675199
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-06
Date of Report2020-02-20
Date of Event2020-01-08
Date Facility Aware2020-01-08
Report Date2020-01-10
Date Reported to Mfgr2020-01-10
Date Mfgr Received2020-01-10
Device Manufacturer Date2010-03-31
Date Added to Maude2020-02-06
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 Location3
Manufacturer ContactMR. JASON WHITTLE
Manufacturer StreetNEWMAINS AVENUE INCHINNAN BUSINESS PARK
Manufacturer CityRENFREWSHIRE, PA4 9RR
Manufacturer CountryUK
Manufacturer PostalPA4 9RR
Manufacturer G1VASCUTEK LTD.
Manufacturer StreetNEWMAINS AVENUE INCHINNAN BUSINESS PARK
Manufacturer CityRENFREWSHIRE, PA4 9RR
Manufacturer CountryUK
Manufacturer Postal CodePA4 9RR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGELSOFT ERS
Generic NameGELSOFT AX-BIFEM EQUI-FLO ERS REINFORCED,
Product CodeDSY
Date Received2020-02-06
Returned To Mfg2020-01-28
Model NumberGELSOFT
Catalog Number691008B
Lot Number108814
Device Expiration Date2015-03-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age10 YR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerVASCUTEK LTD.
Manufacturer AddressNEWMAINS AVENUE INCHINNAN BUSINESS PARK RENFREWSHIRE, PA4 9RR UK PA4 9RR


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-06

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