MAUDE Adverse Event Report: ASAHI INTECC PROWATER; GUIDE WIRE

Model Number	N/A
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	06/25/2021
Type of Reportable Event	Malfunction
Event or Problem Description
Tried to cross mid lad cto with prowater tip broke off tried to retrieve with retrievable device end up stenting over the tip portion to keep in place.No complications.

• Brand Name: PROWATER
• Common Device Name: GUIDE WIRE
• Manufacturer (Section D): ASAHI INTECC; 3-100 akatsuki-cho; seto, aichi 489-0 071; JA 489-0071
• MDR Report Key: 12122687
• Report Number: 3004718255-2021-00227
• Device Sequence Number: 3397788
• Product Code: DQX
• UDI-Device Identifier: 14547327056127
• UDI-Public: (01)14547327056127(17)231231(10)210127A10A
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 06/25/2021
• Report Date (Section F): 07/06/2021

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 Expiration Date: 12/31/2023
• Device Model Number: N/A
• Device Catalogue Number: AGH146000
• Device Lot Number: 210127A10A
• Was Device Available for Evaluation?: Yes
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 06/25/2021
• Device Age: 5 MO
• Event Location: Hospital
• Date Report to Manufacturer: 07/06/2021
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 07/06/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Date Report Sent to FDA: 07/06/2021