MAUDE MDR 9383478

MDR report key
9383478
Report number
MW5091317
Event key
0
Event type
3
Date of event
2019-11-21
Date received
2019-11-26
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
306
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Report source
P
Manufacturer link flag
N

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1BEDWETTING ALARMALARM, CONDITIONED RESPONSE ENURESISMALEM MEDICAL LTD.KPNULTIMATEI Y

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-11-2601. R

Event Narratives#

No narrative records found.