BURLINGTON MEDICAL EURO

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-12 for BURLINGTON MEDICAL EURO manufactured by Burlington Medical.

MAUDE Entry Details

Report Number1222742-2019-00008
MDR Report Key8693061
Date Received2019-06-12
Date of Report2019-05-14
Date Mfgr Received2018-11-08
Device Manufacturer Date2016-11-30
Date Added to Maude2019-06-12
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. JOHN DASPIT
Manufacturer Street7 ELMHURST DR
Manufacturer CityNEWPORT NEWS VA 23603
Manufacturer CountryUS
Manufacturer Postal23603
Manufacturer Phone7579685846
Manufacturer G1BURLINGTON MEDICAL
Manufacturer Street7 ELMHURST ST
Manufacturer CityNEWPORT NEWS VA 23603
Manufacturer CountryUS
Manufacturer Postal Code23603
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBURLINGTON MEDICAL
Generic NameLEAD APRON
Product CodeEAJ
Date Received2019-06-12
Model NumberEURO
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBURLINGTON MEDICAL
Manufacturer Address7 ELMHURST ST. NEWPORT NEWS VA 23603 US 23603


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-12

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