24 results · 25ms · Sources: EU EUDAMED, US FDA

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PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195X

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

MASIMO SET RADICAL PULSE OXIMETER WITH SATSHARE AND LNOP SERIES OF SENSORS AND CABLES

FDA 510(k)
FDA Class 2 ·Cardiovascular

MODEL7500 MICROCURRENT TENS DEVICE, MCT-F5, MCT-F50, MCT-F500

FDA 510(k)
FDA Class 2 ·Neurology

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 6, 2010

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·September 27, 2010

SMARTSITE NEEDLE-FREE VALVE

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FPA·March 13, 2013

RECOVERY ROOM STRETCH OBS 5/97

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FPO·March 15, 2011

CONTAK RENEWAL 3

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 5, 2012

ISA CO2

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 30, 2022

OT ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 18, 2012

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·October 6, 2011

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 10, 2012

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 10, 2012

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 29, 2010

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 25, 2011

OT TEST STRIPS BLUE

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·July 27, 2011

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 23, 2012

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 21, 2011

MEDTRONIC NAVIGATION

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code GEX·May 29, 2020