1,723 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Alira Medical Devices
FDA UDI
Alira Medical Devices, LLC·G767KSR1010·KILNER SKIN RETRACTOR | SHARP
Alira Medical Devices
FDA UDI
Alira Medical Devices, LLC·G767KSR1020·KILNER SKIN RETRACTOR | BLUNT
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613090425·K-Wire/Steinmann Pin Sterilization Rack
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902112153·Epidural Catheteriztion Kit
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902112146·Epidural Catheterization Kit
MICRONY K SR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·January 10, 2004
MICRONY K SR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 6, 2014
MICRONY K SR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 10, 2014
MICRONY K SR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 15, 2014
MICRONY K SR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC CRMD·Product code LWP·January 13, 2014
MICRONY K SR
FDA Adverse Event
Injury
·ST JUDE MEDICAL AB·Product code DXY·March 10, 2006
MICRONY K SR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2006
KAPPA KSR 401
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·May 10, 2023
MICRONY K SR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·July 9, 2002
MICRONY K SR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·April 24, 2003
MICRONY K SR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·March 5, 2015
MEDTRONIC KAPPA KSR 401 GENERATOR
FDA Adverse Event
Injury
·MEDTRONIC INC.·Product code DXY·January 30, 2002
MEDTRONIC KAPPA 700 KSR 701
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·October 27, 2000
TERUFLEX
FDA Adverse Event
TERUMO BCT·Product code KSR·August 13, 2012
2535K MICRONY K, SR, PKGD/STER
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·July 12, 2018