7,388 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Q-SYTE CLOSED LUER ACCESS DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·May 14, 2021
CONNECTA Q-SYTE WHT
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·April 20, 2021
BD NEXIVA KIT W/ Q-SYTE 22GA 1.0IN
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·February 10, 2021
BD NEXIVA¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 5, 2022
Q-SYTE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY·Product code FPA·February 9, 2024
Q TIPS
FDA Adverse Event
Injury
·UNILEVER·Product code KXG·September 24, 2014
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·December 3, 2019
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 26, 2015
UNSPECIFIED BD Q-SYTE LUER ACCESS
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·December 23, 2021
BD Q-SYTE¿ TRI-EXTENSION SET
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·May 30, 2023
BD Q-SYTE LUER ACCESS SPLIT SEPTUM
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·February 17, 2022
BD Q-SYTE LUER ACCESS SPLIT-SEPTUM
FDA Adverse Event
Other
·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FPA·March 23, 2010
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS: 532 AND 1064 ND:YAG HANDPIECE ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD EXT SET 15CM SMALL BORE SPIN NUT
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·March 1, 2024
DIMENSION VISTA 500
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 7, 2016
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 25, 2019
BD Q-SYTE LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 20, 2020