31 results · 22ms · Sources: EU EUDAMED, US FDA

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LCS FEMORAL HIP PROSTHESIS

FDA 510(k)
FDA Class 2 ·Orthopedic

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575256532·Articulating Surfaces, PS+

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575256495·Articulating Surfaces, PS+

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575256501·Articulating Surfaces, PS+

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575256518·Articulating Surfaces, PS+

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575256488·Articulating Surfaces, PS+

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575256525·Articulating Surfaces, PS+

Cadwell Apollo System

FDA 510(k)
FDA Class 2 ·Neurology

TRIAGE CARDIOPROFILER AND PROFILER S.O.B. PANELS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

TRIAGE PROFILER SOB PANEL 25T

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·July 19, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Injury ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 13, 2019

TRIAGE PROFILER SOB PANEL 25T

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code JHX·August 29, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·March 4, 2021

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 3, 2018

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·January 25, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 23, 2019

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 18, 2014

SHILEY DISPOSABLE CANNULA LOW PRESSURE

FDA Adverse Event
Injury ·COVIDIEN/ FORMERLY TYCO HEALTHCARE·Product code JOH·October 19, 2010

COBAS AMPLIPREP / COBAS AMPLICOR HCV TEST, V2.0 CE-IVD

FDA Adverse Event
ROCHE MOLECULAR SYSTEMS·Product code MZP·December 19, 2012

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 5, 2018