MAUDE Adverse Event Report: CONMED CORPORATION SUREFIT; ELECTROSURGICAL, CUTTING COAGULATION ACCESSORIES

Model Number	410-2000
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/30/2023
Type of Reportable Event	Malfunction
Event or Problem Description
Bovie pad fully adhered to patient's skin, however, bovie machine alarming disconnected pad.Bovie machine cleared via medical engineering as working appropriately.

• Brand Name: SUREFIT
• Common Device Name: ELECTROSURGICAL, CUTTING COAGULATION ACCESSORIES
• Manufacturer (Section D): CONMED CORPORATION; 525 french rd; utica NY 13502
• MDR Report Key: 16768362
• Report Number: 16768362
• Device Sequence Number: 15047397
• Product Code: GEI
• UDI-Device Identifier: 30653405033831
• UDI-Public: (01)30653405033831
• Combination Product (Y/N): N
• Initial Reporter State: RI
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: User Facility
• Initial Reporter Occupation: Risk Manager
• Type of Report: Initial
• Report Date (Section B): 03/30/2023
• Report Date (Section F): 03/30/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 410-2000
• Device Catalogue Number: 410-2000
• Device Lot Number: 202209214
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: Yes
• Event Location: Hospital
• Date Report to Manufacturer: 04/19/2023
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 04/19/2023
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Female
• Date Report Sent to FDA: 03/30/2023