235 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ZYNERGY Z3K BALLOON GUIDED PACING AND MONITORING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Vivid Nano Fill Unit Dose Assorted
FDA UDI
PEARSON DENTAL SUPPLIES, INC.·D724D0100990·4g x 4
MEGA PLUS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809763501920·Final Wrench (BT20)
MEDICON, E.G.
FDA registration
MEDICON, E.G.·184 products·🇩🇪 Germany
InTess C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07309K0100090·Tamp, Oblique Kicker
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100090·Dilator Sleeve, Screwdriver
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100190·SNII Tap, 7.50mm
Cosmolock
FDA UDI
Kalitec Direct LLC·B07310K0100290·Caddie Lid, MIS Rods and Caps
CAMLOG SCREW IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
KOKO PEAK KP; KOKO PEAK KP+
FDA 510(k)
FDA Class 2
·Anesthesiology
8010099-2009-00001
FDA Adverse Event
Malfunction
·Product code GAD·January 26, 2009
8010099-2007-00001
FDA Adverse Event
Other
·Product code GAD·February 2, 2007
8010099-2008-00002
FDA Adverse Event
Malfunction
·Product code GAD·July 2, 2008
8010099-2008-00001
FDA Adverse Event
Malfunction
·Product code GEI·February 20, 2008
BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 25, 2021
BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 28, 2026
BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 21, 2026
BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026
BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 20, 2026