24 results · 23ms · Sources: EU EUDAMED, US FDA

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EchoSolv AS

FDA 510(k)
FDA Class 2 ·Radiology

J & J INSTRUMENTS

FDA UDI
J & J INSTRUMENTS INC·00817524026108·CRILE FCP 5.5"" CVD

ETEX MIXING AND DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

PTA Balloon Dilatation Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD INSYTE AUTOG BC WING

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 5, 2024

BD INSYTE AUTOG BC WING

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 5, 2024

BD INSYTE AUTOG BC WING

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 6, 2024

SPIDERFX EMBOLIC PROTECTION DEVICE

FDA Adverse Event
Injury ·EV3 INC.·Product code NTE·November 7, 2008

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 18, 2011

DIMENSION® CLINICAL CHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code MLM·July 22, 2013

SPECTRA OPTIA

FDA Adverse Event
Injury ·TERUMO BCT·Product code GKT·June 2, 2017

SPECTRA OPTIA

FDA Adverse Event
Injury ·TERUMO BCT·Product code LKN·June 2, 2017

COBE SPECTRA BLOOD COLLECTION

FDA Adverse Event
Injury ·TERUMO BCT·Product code GKT·May 30, 2017

PIPELINE EMBOLIZATION DEVICE

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code OUT·December 18, 2013

PINN MULTIHOLE W/GRIPTION 50MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 15, 2023

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·March 1, 2018

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·March 1, 2018

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 22, 2015

BD INSYTE AUTOG BC WING

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 12, 2024

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·June 1, 2017