8 results
·
33ms
·
Sources: EU EUDAMED, US FDA
ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
OSTYCUT BONE BIOPSY NEEDLE
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code DWO·September 7, 2015
GC Initial™
FDA UDI
Gc America Inc.·J0228745851·GC Initial™ Ti Enamel Occlusal EO-15, 50g
CELLTRAK-B
FDA 510(k)
FDA Class 2
·General Hospital
REFERRIL CALIBRATORS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·December 15, 2012
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·June 16, 2014