12 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PB3300 SENSING CATHETER FOR CONTINUOUS MEASUREMENT
FDA 510(k)
FDA Class 2
·Anesthesiology
"2.4MM" SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036053598·
MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
NOVABONE DENTAL MORSELS - BIOACTIVE SYNTHETIC BONE GRAFT
FDA 510(k)
FDA Class 2
·Dental
LC4200 PCA PLUS AUST
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·March 8, 2012
LC4200 PCA AUST
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code MEA·October 20, 2010
PCA PUMP (AUZ)
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code MEA·March 13, 2012
LC4200 PCA PLUS AUST
FDA Adverse Event
Injury
·HOSPIRA COSTA RICA LTD.·Product code MEA·March 1, 2012
PCA PUMP (AUZ)
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code MEA·June 2, 2010
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
SHUNLONG PHYSICAL THERAPY EQUIPMENT·Product code ITJ·January 12, 2013
SERVO-S
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·November 16, 2010
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 3, 2014