37 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DLP Aortic Root Cannula, DLP Aortic Root Cannula with Vent Line, DLP Pressure Monitoring Extension Line Adapter, DLP Cardioplegia Adapter with Pressure Port
FDA 510(k)
FDA Class 2
·Cardiovascular
Oticon
FDA UDI
Oticon A/S·05707131334541·OPN 2, KIT 312 2.4G NFM 90 L C001
S9 VPAP ADAPT WITH H5I
FDA 510(k)
FDA Class 2
·Anesthesiology
LIGHTWAVE PROFESSIONAL DELUXE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 31, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 30, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 8, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 23, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 29, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 24, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 27, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 16, 2026
BD PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026
HARMONIC SCALPEL GENERATOR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 3, 2008