23 results
·
28ms
·
Sources: EU EUDAMED, US FDA
MAGNE-DENT
FDA 510(k)
FDA Class 1
·Dental
DUAL CHEST PAD, RIGHT
FDA UDI
MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430101014·
Fresh Cells
FDA UDI
DIAGNOSTIC HYBRIDS, INC.·30014613334156·VERO CELLS TUBE CULT
GENEX BONE GRAFT SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic
SB ANCHOR
FDA 510(k)
FDA Class 2
·Dental
UniTip Catheter
FDA UDI
Unisensor AG·07640172973769·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972427·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971727·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971758·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971741·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971734·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971765·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971772·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971710·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971789·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971703·
M2A-MAGNUM MOD HD SZ 42MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 30, 2014
MINICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·November 20, 2012
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 17, 2010
COMPR SRS PROX BDY - SM 48MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·October 16, 2019