8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
CMV-CUBE(TM)
FDA 510(k)
FDA Class 2
·Microbiology
CHLAMYDIAZYME DIAGNOSTIC KIT
FDA 510(k)
FDA Class 1
·Microbiology
NEOS-LP PULSE GENERATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
DURATA STS OPTIM PASSIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 19, 2014
UNKNOWN
FDA Adverse Event
Injury
·UNK·Product code LJT·October 25, 2010
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 3, 2012
ALARIS PUMP MODULE SET NON-VENTED BLOOD SET
FDA Adverse Event
Malfunction
·Product code FPA·June 29, 2021
BD ALARIS¿ LVP BLD180M 15D SS
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 30, 2020