MAUDE MDR 9631328

MDR report key
9631328
Report number
1220246-2020-01595
Event key
0
Event type
3
Date of event
2020-01-06
Date received
2020-01-27
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
401
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Contact
VIK BAJNATH
Phone
800-800-8009
Report source
M
Manufacturer link flag
Y

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1MONITOR, 4K, UHD4, 32 ,"CAMERA, SURGICAL AND ACCESSORIESARTHREX, INC.KQMMONITOR, 4K, UHD4, 32 ,"AR-3250-320710169039N Y

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12020-01-2701. O

Event Narratives#

No narrative records found.