ORCAPOD 4 2219-02

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 2019-06-20 for ORCAPOD 4 2219-02 manufactured by Boston Scientific Corporation.

MAUDE Entry Details

Report Number3005099803-2019-03137
MDR Report Key8717538
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-06-20
Date of Report2019-06-20
Date of Event2019-05-28
Date Mfgr Received2019-05-29
Device Manufacturer Date2019-03-19
Date Added to Maude2019-06-20
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 ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY ,
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
Manufacturer G1POLYMER TECHNOLOGIES
Manufacturer Street,
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameORCAPOD 4
Generic NameORCAPOD 4
Product CodeODC
Date Received2019-06-20
Model Number2219-02
Catalog Number2219-02
Lot Number0000458958
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY , MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.