8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
NEISSERIA IDENTIFICATION DISCS
FDA 510(k)
FDA Class 1
·Microbiology
iNSitu Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127026157·Acetabular Reamer, Full Hemisphere, Crossbar, 64mm
VitalFlow Console
FDA 510(k)
FDA Class 2
·Cardiovascular
DEROYAL GOWNS, STERILE, NON-STERILE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 12, 2014
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·November 13, 2012
HARMONIC ACE 36 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·January 14, 2008
NATUS EMBLA NDX AMPLIFIER
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code GWQ·August 26, 2020