MANOSCAN 3890

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-09-17 for MANOSCAN 3890 manufactured by Given Imaging Los Angeles Llc.

Event Text Entries

[120714462] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[120714463] According to the reporter, the catheter was difficult to remove upon extubation but they were able removing it, however, the patient? S nose started to bleed and they were able to stop the bleeding. There was no reported patient outcome.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005344223-2018-00011
MDR Report Key7882728
Report SourceUSER FACILITY
Date Received2018-09-17
Date of Report2018-09-17
Date Mfgr Received2018-08-27
Date Added to Maude2018-09-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactAMY BEEMAN
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone7632104064
Manufacturer G1GIVEN IMAGING LOS ANGELES LLC
Manufacturer Street5860 UPLANDER WAY
Manufacturer CityCULVER CITY CA 90230
Manufacturer CountryUS
Manufacturer Postal Code90230
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMANOSCAN
Generic NameSYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)
Product CodeFFX
Date Received2018-09-17
Model Number3890
Catalog Number3890
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerGIVEN IMAGING LOS ANGELES LLC
Manufacturer Address5860 UPLANDER WAY CULVER CITY CA 90230 US 90230


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-17

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