CHATTANOOGA APPLICATOR 9CLS 5X200MW 1040MW 27812

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 2019-07-09 for CHATTANOOGA APPLICATOR 9CLS 5X200MW 1040MW 27812 manufactured by Djo, Llc.

MAUDE Entry Details

Report Number3012446970-2019-00019
MDR Report Key8772707
Report SourceUSER FACILITY
Date Received2019-07-09
Date of Report2019-07-09
Date of Event2019-06-12
Date Mfgr Received2019-06-12
Device Manufacturer Date2013-05-09
Date Added to Maude2019-07-09
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 ContactMR. BRIAN BECKER
Manufacturer Street2900 LAKE VISTA DRIVE
Manufacturer CityLEWISVILLE TX 75067
Manufacturer CountryUS
Manufacturer Postal75067
Manufacturer G1DJO, LLC
Manufacturer Street3151 SCOTT ST.
Manufacturer CityVISTA CA 920819663
Manufacturer CountryUS
Manufacturer Postal Code920819663
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHATTANOOGA APPLICATOR 9CLS 5X200MW 1040MW
Generic NameLAMP, INFRARED, THERAPEUTIC HEATING
Product CodeILY
Date Received2019-07-09
Returned To Mfg2019-06-13
Model Number27812
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDJO, LLC
Manufacturer Address1430 DECISION STREET VISTA CA 920819663 US 920819663


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-07-09

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