MAUDE MDR 8721569

MDR report key
8721569
Report number
8721569
Event key
0
Event type
3
Date of event
2019-06-09
Date received
2019-06-21
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
100
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
1COMFORT GLIDE LTDEVICE, TRANSFER, PATIENT, MANUALMEDLINE INDUSTRIES, INCFMRMSD600LTMSC600LT2981901000* N

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-06-210

Event Narratives#

No narrative records found.