21 results · 24ms · Sources: EU EUDAMED, US FDA

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PENUMBRA SYSTEM MAX

FDA 510(k)
FDA Class 2 ·Cardiovascular

JOBST forMen Casual

FDA UDI
BSN MEDICAL, INC.·00035664005696·FOR MEN CASUAL 30-40 MM HG KNEE HIGH CLOSED TOE...

UNIGLOVE LANO-E POWDER-FREE LATEX EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

APPROACH PRO ST WIRE GUIDE

FDA 510(k)
FDA Class 2 ·Cardiovascular

AUTODISC 50 TEST STRIPS

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·May 25, 2007

ASCENSIA BREEZE2

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 14, 2007

AUTODISC 100 TEST STRIPS

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·September 15, 2006

AUTODISC 50 TEST STRIPS

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·May 8, 2007

ASCENSIA BREEZE

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 20, 2007

AUTODISC 50 TEST STRIPS

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·March 21, 2007

BREEZE2

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·August 18, 2009

T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 19, 2024

ASCENSIA BREEZE

FDA Adverse Event
Injury ·BAYER HEALTHCARE, LLC·Product code CGA·December 1, 2005

AUTODISC 50 TEST STRIPS

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·August 15, 2008

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 5, 2015

VILEX

FDA Adverse Event
Malfunction ·VILEX, INC.·Product code JDW·June 4, 2012

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS INC.·Product code CBK·May 9, 2013

ONCOTYPE DX MULTIVARIATE INDEX

FDA Adverse Event
Injury ·GENOMIC HEALTH·Product code NPQ·May 27, 2011

COZMO INSULIN PUMP

FDA Adverse Event
Injury ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code LZG·August 12, 2008

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 12, 2016