Device-Related Adverse Events and Modes of Failure in Renal Denervation Systems: Insights From the Food and Drug Administration Manufacturer and User Facility Device Experience (FDA MAUDE) Database Analysis.
- DOI
- 10.7759/cureus.96770
- Published
- 2025 Nov
- Container
- Cureus
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.7759/cureus.96770,
title = {Device-Related Adverse Events and Modes of Failure in Renal Denervation Systems: Insights From the Food and Drug Administration Manufacturer and User Facility Device Experience (FDA MAUDE) Database Analysis.},
author = {Jasti M and Kumar A and Nanjundappa A and Kalra A and Paul T},
year = {2025},
journal = {Cureus},
doi = {10.7759/cureus.96770},
url = {https://doi.org/10.7759/cureus.96770}
}RIS
TY - JOUR TI - Device-Related Adverse Events and Modes of Failure in Renal Denervation Systems: Insights From the Food and Drug Administration Manufacturer and User Facility Device Experience (FDA MAUDE) Database Analysis. AU - Jasti M AU - Kumar A AU - Nanjundappa A AU - Kalra A AU - Paul T PY - 2025 JO - Cureus DO - 10.7759/cureus.96770 UR - https://doi.org/10.7759/cureus.96770 ER -
APA
M, J., A, K., A, N., A, K., & T, P. (2025). Device-Related Adverse Events and Modes of Failure in Renal Denervation Systems: Insights From the Food and Drug Administration Manufacturer and User Facility Device Experience (FDA MAUDE) Database Analysis.. Cureus. https://doi.org/10.7759/cureus.96770
Source records
- pubmed · retrieved 2026-09-26T22:31:05.101Z