9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
SURGICAL SUCTION INSTRUMENTS-DISPOS.
FDA 510(k)
FDA Class 2
·General Hospital
CoRoent
FDA UDI
Nuvasive, Inc.·00887517368126·CoRoent® XL Ti, 12x18x45mm
ERA® Implant Abutment Micro 0°, 2mm Cuff (AP)
FDA UDI
STERNGOLD DENTAL LLC·00841549105159·Implant retained overdentures are an establishe...
MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
SIMPLICITY SOFT QD MICRO INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
UNSPECIFIED BD NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·October 20, 2020
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·April 25, 2014
MAXIMO II CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·August 12, 2010