9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MODEL 2 FLOWMETER
FDA 510(k)
FDA Class 1
·Anesthesiology
MUSE CARDIOLOGY INFORMATION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4
FDA 510(k)
FDA Class 2
·Dental
SYRINGE S2 5ML 22GA 1-1/4IN BD CHINA
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·July 10, 2019
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014
ALTRX +4 NEUT 32IDX50OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·October 31, 2012
PREMIUM SURGICLIP S-9.0 TITANIUM
FDA Adverse Event
Injury
·USSC PUERTO RICO·Product code GDO·August 17, 2010
BD SYRINGE S2 5ML 22GA 1-1/4IN BD CHINA
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 30, 2019
BD SYRINGE S2 5ML 22GA 1-1/4IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 26, 2019