CYTOLOGY BRUSH 60314 109265602

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 2020-02-25 for CYTOLOGY BRUSH 60314 109265602 manufactured by Avanos Medical Inc..

MAUDE Entry Details

Report Number8030647-2020-00020
MDR Report Key9751888
Report SourceUSER FACILITY
Date Received2020-02-25
Date of Report2020-03-09
Date Mfgr Received2020-03-02
Device Manufacturer Date2019-05-22
Date Added to Maude2020-02-25
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 ContactMS. LISA CLARK
Manufacturer Street5405 WINDWARD PARKWAY
Manufacturer CityALPHARETTA GA 30004
Manufacturer CountryUS
Manufacturer Postal30004
Manufacturer Phone4704485444
Manufacturer G1AVENT S DE RL DE CV
Manufacturer StreetCARRETERA INTERNACIONAL SALIDA NORTE NO. 1053
Manufacturer CityMAGDALENA, CP
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCYTOLOGY BRUSH
Generic NameDH ENDOSCOPY GRASPING & RETRIEVING DEVICES
Product CodeFDX
Date Received2020-02-25
Returned To Mfg2020-03-02
Model Number60314
Catalog Number109265602
Lot NumberM19140E102
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerAVANOS MEDICAL INC.
Manufacturer Address5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-25

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