MAUDE Adverse Event Report: FERROSAN MEDICAL DEVICES A/S; SURGIFLO® HEMOSTATIC MATRIX

Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Wound Dehiscence (1154)
Type of Reportable Event	Serious Injury
Event or Problem Description
Per user facility medwatch form #mw5153569 and mw5153570*, during an unknown procedure, there was vaginal cuff dehiscence.There were no patient consequences reported.Procedure date: (b)(6) 2024 event date: (b)(6) 2024.

• Common Device Name: SURGIFLO® HEMOSTATIC MATRIX
• Manufacturer (Section D): FERROSAN MEDICAL DEVICES A/S; sydmarken 5; soeborg, 2860 ; DA 2860
• MDR Report Key: 19248401
• Report Number: 3008478369-2024-00020
• Device Sequence Number: 6397005
• Product Code: LMF
• UDI-Device Identifier: 25712123000315
• UDI-Public: 25712123000315
• Combination Product (Y/N): N
• PMA/510(K) Number: P990004
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/06/2024
• Patient Sequence Number: 1
• Patient Sex: Unknown