69 results · 34ms · Sources: EU EUDAMED, US FDA

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FemVue® Controlled Saline-Air Device (FSA-300)

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575305704·Knee femur prosthesis trial - Endo Model Knee S...

LUCAS

FDA 510(k)
FDA Class 2 ·Cardiovascular

Aptiva CTD Essential Reagent

FDA 510(k)
FDA Class 2 ·Immunology

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 18, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 18, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 20, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·April 21, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 20, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·May 28, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 28, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 15, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 11, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 14, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·April 21, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 11, 2026

NEXIVA MAXZERO

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 15, 2026

NEXIVA

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 18, 2026

HYDROFLEX HD HYSTEROSCOPIC DISTENTION TUBING SET

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code HIG·December 3, 2008

ASR ACETABULAR IMPLANT 58

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·September 19, 2011