MONOMAX VIOLET 1(4)150CM HRT48 LOOP(M B0041222

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 2019-06-04 for MONOMAX VIOLET 1(4)150CM HRT48 LOOP(M B0041222 manufactured by B.braun Surgical Sa.

MAUDE Entry Details

Report Number3003639970-2019-00453
MDR Report Key8668591
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-06-04
Date of Report2019-06-04
Date Facility Aware2019-05-22
Date Mfgr Received2019-05-08
Date Added to Maude2019-06-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. LINDSAY CHROMIAK
Manufacturer Street3773 CORPORATE PARKWAY
Manufacturer CityCENTER VALLEY PA 18034
Manufacturer CountryUS
Manufacturer Postal18034
Manufacturer Phone8002581946
Manufacturer G1B/ BRAUN SURGICAL SA
Manufacturer Street121 CARRETERA DE TERRASSA
Manufacturer CityRUBI, 08191
Manufacturer CountrySP
Manufacturer Postal Code08191
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMONOMAX VIOLET 1(4)150CM HRT48 LOOP(M
Generic NameSYNTHETIC ABSORBABLE MONOFILAR
Product CodeNWJ
Date Received2019-06-04
Returned To Mfg2019-05-15
Model NumberB0041222
Catalog NumberB0041222
Lot Number118516
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerB.BRAUN SURGICAL SA
Manufacturer Address121 CARRETERA DE TERRASSA RUBI, 08191 SP 08191


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-04

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