INTRAOPERATRIVE PROBE COVER PC1290

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,user facility report with the FDA on 2019-06-03 for INTRAOPERATRIVE PROBE COVER PC1290 manufactured by Ecolab.

MAUDE Entry Details

Report Number8043817-2019-40021
MDR Report Key8662787
Report SourceCONSUMER,USER FACILITY
Date Received2019-06-03
Date of Report2019-06-03
Date of Event2019-05-16
Date Added to Maude2019-06-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINTRAOPERATRIVE PROBE COVER
Generic NamePROBE COVER
Product CodeKKX
Date Received2019-06-03
Model NumberPC1290
Lot NumberD190229
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerECOLAB
Manufacturer Address1 ECOLAB PLACE ST PAUL MN 55102 US 55102


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-06-03

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