20 results · 23ms · Sources: EU EUDAMED, US FDA

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CROSSER LP SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014607344·SKYTRON 3501B 5.25" DELUXE GEL

NA

FDA UDI
STRYKER CORPORATION·07613327056624·Sliding-Lock Atraumatic Grasper, Single Action.

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009

MICROVASIVE ZERO TIP AIRWAY RETRIEVAL BASKET, MODELS M00513200 AND M00513210

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

COULTER HMX ANALYZER, MODEL 6605523, COULTER HMX WITH AUTOLOADER, MODEL 6605526

FDA 510(k)
FDA Class 2 ·Hematology

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·July 20, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·January 5, 2016

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 26, 2010

EDWARDS TRANSFEMORAL BALLOON CATHETER

FDA Adverse Event
Death ·EDWARDS LIFESCIENCES·Product code NPT·April 26, 2013

OT ULTRAMINI METER

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

ABACUS V2.0 TPN CALCULATING SOFTWARE

FDA Adverse Event
Injury ·BAXA CORP.·Product code LNX·July 23, 2008

COULTER ISOTON III DILUENT

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GIF·May 1, 2014

COULTER ISOTON III DILUENT

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GIF·April 28, 2014

COULTER ISOTON III DILUENT

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GIF·March 27, 2014

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·July 20, 2009

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·November 13, 2015