MAUDE Adverse Event Report: RADIOMETER MEDICAL APS AQURE

Model Number	933-599
Medical Device Problem Codes	Communication or Transmission Problem (2896); Patient Data Problem (3197)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/04/2025
Type of Reportable Event	Malfunction
Event or Problem Description
Radiometer complaint reference: (b)(4).According to the complaint, on (b)(6) 2025, the customer experienced incorrect value display in aqure.Sample type parameter "fibtem c" was sent as "---" (indicating an invalid or missing result) is displayed as an incorrect numerical value in the aqure web interface.No reports of death or serious injury.
Additional Manufacturer Narrative
Radiometer preliminary investigations have suggested that the customer should upgrade to an aqure/driver version where the issue is fixed.
Additional Manufacturer Narrative
The investigation has shown that the device did not malfunction.Therefore, this incident does not meet the criteria for a reportable mdr.

• Brand Name: AQURE
• Common Device Name: AQURE
• Manufacturer (Section D): RADIOMETER MEDICAL APS; aakandevej 21; broenshoej, 2700 ; DA 2700
• Manufacturer (Section G): RADIOMETER MEDICAL APS; aakandevej 21; broenshoej, 2700 ; DA 2700
• Manufacturer Contact: pearlyn pah ; aakandevej 21; broenshoej, 2700 ; DA 2700
• MDR Report Key: 23616065
• Report Number: 3002807968-2025-00137
• Device Sequence Number: 15695426
• Product Code: OUG
• UDI-Device Identifier: 05700699335999
• UDI-Public: (01)05700699335999
• Combination Product (Y/N): N
• Initial Reporter Country: SW
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/16/2025

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: 933-599
• Device Catalogue Number: 933-599
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/07/2025
• Supplement Date Received by Manufacturer: 11/26/2025
• Initial Report FDA Received Date: 11/21/2025
• Supplement Report FDA Received Date: 12/15/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown