32 results
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55ms
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Sources: EU EUDAMED, US FDA
Peptonic Medical AB
FDA registration
Peptonic Medical AB·1 product·🇸🇪 Sweden
MedNet EC-REP GmbH
Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices
AUTOPULSE RESUSCITAITON SYSTEM MODEL 100
FDA Adverse Event
Death
·ZOLL CIRCULATION, INC.·Product code DRM·May 13, 2013
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·September 22, 2012
POWERED WHEELCHAIR
FDA Adverse Event
INVACARE TAYLOR STREET·Product code ITI·November 6, 2012
ORTHO REAGENT RED BLOOD CELLS 0.8% SELECTOGEN
FDA Adverse Event
Injury
·ORTHO CLINICAL DIAGNOSTICS·Product code KSZ·December 9, 2015
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·January 26, 2017
PERI-GUARD PERICARDIUM WITH APEX PROCESSING
FDA Adverse Event
Death
·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·February 6, 2014
PLENITY
FDA Adverse Event
Injury
·GELESIS SRL·Product code QFQ·August 18, 2021
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 17, 2018
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·June 14, 2012
FLOSEAL HEMOSTATIC MATRIX
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - HAYWARD·Product code LMF·October 14, 2011
FLOSEAL HEMOSTATIC MATRIX
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - HAYWARD·Product code LMF·May 23, 2011
NOVOPEN 4
FDA Adverse Event
Injury
·NOVO NORDISK A/S·Product code FMF·October 2, 2015
VERITAS COLLAGEN MATRIX
FDA Adverse Event
Injury
·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·February 21, 2014
FLOSEAL
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - HAYWARD·Product code LMF·November 5, 2010
COSEAL SURGICAL SEALANT
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - HAYWARD·Product code NBE·June 25, 2011
FLOSEAL HEMOSTATIC MATRIX
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - HAYWARD·Product code LMF·May 2, 2011
HYALGAN
FDA Adverse Event
Injury
·FIDIA FARMACEUTICI S.P.A.·Product code MOZ·June 30, 2017
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·February 26, 2010