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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