8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Blood Administration Sets
FDA 510(k)
FDA Class 2
·General Hospital
ELMED
FDA UDI
ELMED INCORPORATED·00842180120969·5 MM DIA., 33 CM INSULATED SPATULA ELECTRODE, S...
LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE
FDA 510(k)
FDA Class 2
·Neurology
ONETOUCH REVEAL DIABETES MANAGEMENT APPLICATION
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ADVIA CENTAUR TROPONIN ULTRA ASSAY
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·October 30, 2008
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 18, 2011
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·April 21, 2021