MAUDE Adverse Event Report: Oscor Inc. Occlutech Delivery Set III; INTRODUCER, CATHETER

Model Number	98DS011
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/24/2026
Type of Reportable Event	Malfunction

• Brand Name: Occlutech Delivery Set III
• Common Device Name: INTRODUCER, CATHETER
• Manufacturer (Section D): Oscor Inc.; 4875 palm harbor blvd.; palm harbor FL 34683
• Manufacturer (Section G): Oscor Inc.; 4875 palm harbor blvd.; palm harbor FL 34683
• Manufacturer Contact: mohit malkani ; 4875 palm harbor blvd.; palm harbor, FL 34683 ; +1(727)937-2511
• MDR Report Key: 50057436
• Report Number: 1035166-2026-00053
• Device Sequence Number: 10665698
• Product Code: DYB
• UDI-Device Identifier: 00885672010331
• UDI-Public: 00885672010331
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K210627
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/11/2026

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: 98DS011
• Device Catalogue Number: 98DS011
• Device Lot Number: DP-21413
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 08/25/2026
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 06/24/2026
• Supplement Date Received by Manufacturer: 08/25/2026
• Initial Report FDA Received Date: 07/28/2026
• Supplement Report FDA Received Date: 09/11/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/22/2024
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown