MAHURKAR ELITE 8888211416

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-17 for MAHURKAR ELITE 8888211416 manufactured by Covidien Mfg Solutions S.a..

Event Text Entries

[175373912] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[175373913] According to the reporter, the guidewire was unraveled. They were able to pull it out of the patient and perform a scan to be sure that not was left.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009211636-2020-00018
MDR Report Key9601119
Report SourceUSER FACILITY
Date Received2020-01-17
Date of Report2020-01-17
Date Mfgr Received2019-12-31
Device Manufacturer Date2019-03-01
Date Added to Maude2020-01-17
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 ContactLISA HERNANDEZ
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone2034925563
Manufacturer G1COVIDIEN MFG SOLUTIONS S.A.
Manufacturer StreetEDIFICIO B20, CALLE #2
Manufacturer CityALAJUELA 20101
Manufacturer Postal Code20101
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAHURKAR ELITE
Generic NameCATHETER, HEMODIALYSIS, NON-IMPLANTED
Product CodeMPB
Date Received2020-01-17
Model Number8888211416
Catalog Number8888211416
Lot Number1835100092
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN MFG SOLUTIONS S.A.
Manufacturer AddressEDIFICIO B20, CALLE #2 ALAJUELA 20101 20101


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-17

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