FDA.reportPublic FDA data

MAUDE MDR 8926207

MDR report key
8926207
Report number
8926207
Event key
0
Event type
3
Date of event
2019-07-31
Date received
2019-08-23
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
2
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Report source
U
Manufacturer link flag
N

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1PREMIERPRO PLUSPOWDER-FREE NITRILE PATIENT EXAMINATION GLOVESVS LLCLZC50635063MTH12-16* Y

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-08-230

Event Narratives#

No narrative records found.