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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Philips Medical Systems Nederland B.V. Allura Xper FD; system, x-ray, angiographic

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Philips Medical Systems Nederland B.V. Allura Xper FD; system, x-ray, angiographic Back to Search Results
Model Number Allura Xper FD20
Medical Device Problem Code Radiation Output Failure (4027)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 09/16/2026
Type of Reportable Event Malfunction
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Brand Name
Allura Xper FD
Common Device Name
system, x-ray, angiographic
Manufacturer (Section D)
Philips Medical Systems Nederland B.V.
veenpluis 6
best 5684 PC
NL  5684 PC
Manufacturer (Section G)
Philips Medical Systems Nederland B.V.
veenpluis 6
best 5684 PC
NL   5684 PC
Manufacturer Contact
marjan vos
veenpluis 6
best 5684 -PC
NL   5684 PC
MDR Report Key50929613
Report Number3042175844-2026-002653
Device Sequence Number16137239
Product Code IZI
UDI-Device Identifier00884838059054
UDI-Public(01)00884838059054
Combination Product (Y/N)N
Initial Reporter CountryCH
PMA/510(K) Number
K130842
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,User Facility,Company Representative
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 09/29/2026
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 NumberAllura Xper FD20
Device Catalogue Number722012
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 09/16/2026
Initial Report FDA Received Date09/29/2026
Date Device Manufactured11/28/2017
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 Number1
Patient SexUnknown
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