MAUDE MDR 9145734

MDR report key
9145734
Report number
9145734
Event key
0
Event type
3
Date of event
2019-07-25
Date received
2019-10-02
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
1KENDALL SCDSLEEVE, LIMB, COMPRESSIBLECARDINAL HEALTH, INC.JOWUH29525UH29525* *

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-10-020

Event Narratives#

No narrative records found.