736 results
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32ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ULTIMA SNORING MIKE, MODEL 0540
FDA 510(k)
FDA Class 2
·Anesthesiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040109875·OBTURATOR - OBT6 - SIZE 45 Obt 6pk - CHC4.5
Midway Select
FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717103117·Midway Select Disposable Diamonds 856-016C-S, P...
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113164·PS Insert, Size 3 x 12mm
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0103120·Shaver, Closed, 12mm
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345024076·Paddle Shaver, 12mm
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 4, 2025
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 23, 2026
VARELISA SM ANTIBODIES
FDA 510(k)
FDA Class 2
·Immunology
PROTON VISION 7.0
FDA 510(k)
FDA Class 2
·Radiology
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 22, 2024
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 21, 2024
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 31, 2024
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 23, 2025
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·February 21, 2024
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 7, 2024
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 23, 2025
BD PHOENIX¿ AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·December 22, 2023
DIMENSION RXL MAX WITH HM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MMI·March 25, 2013
NONE
FDA Adverse Event
Other
·INTEGRA, BIOT·Product code JXG·March 11, 2011