1,723 results · 26ms · Sources: EU EUDAMED, 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