15 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Sinusway Dilation System
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780362678·Integra® Miltex® Barraquer Needle Holder, 5", C...
VTS1000
FDA 510(k)
FDA Class 1
·General Hospital
GISH VISION BLOOD CARDIOPLEGIA WITH HA COATING
FDA 510(k)
FDA Class 2
·Cardiovascular
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·August 11, 2021
2210968-2011-00659
FDA Adverse Event
Injury
·ETHICON INC.·July 28, 2011
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·June 14, 2013
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 17, 2014
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·August 26, 2021
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·August 11, 2021
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·August 18, 2021
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·August 27, 2021
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·August 30, 2021
VERISET
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code LMG·July 9, 2018
VERISET
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code LMG·July 9, 2018