UNKNOWN COOLED RF PROBES AND CANNULAS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,litera report with the FDA on 2020-02-17 for UNKNOWN COOLED RF PROBES AND CANNULAS manufactured by Avanos Medical Inc..

MAUDE Entry Details

Report Number8030647-2020-00016
MDR Report Key9717591
Report SourceCOMPANY REPRESENTATIVE,LITERA
Date Received2020-02-17
Date of Report2020-02-17
Date Mfgr Received2020-01-27
Date Added to Maude2020-02-17
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 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 84160
Manufacturer CountryMX
Manufacturer Postal Code84160
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN COOLED RF PROBES AND CANNULAS
Generic NameCOOLED RF PROBES AND CANNULAS
Product CodeGXI
Date Received2020-02-17
Model NumberUNKNOWN
Catalog NumberUNKNOWN
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAVANOS MEDICAL INC.
Manufacturer Address5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-17

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