MAUDE MDR 8731363

MDR report key
8731363
Report number
MW5087594
Event key
0
Event type
3
Date of event
2019-04-28
Date received
2019-06-24
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
3
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
1RADSPEED GENERAL X-RAY SYSTEMSYSTEM, X-RAY, STATIONARYSHIMADZU MEDICAL SYSTEMSKPRRADSPEEDI Y

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-06-240

Event Narratives#

No narrative records found.