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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