42 results
·
44ms
·
Sources: EU EUDAMED, US FDA
Arthroscope Reprocessed Arthroscopic Blades (Arthroscopic Blades and Burrs)
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Reprocessed Arthroscopic Cutters
FDA registration
Stryker Sustainability Solutions Lakeland·1 product·🇺🇸 United States
FAT PROCESSING KIT
FDA registration
ALIRA MEDICAL DEVICES LLC·1 product·🇺🇸 United States
PURE SCULPT POWER CANNULA SYSTEM
FDA registration
KMI IMI GROUP / DBA: INNOVATIVE MED, INC.·1 product·🇺🇸 United States
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151224·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151231·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151194·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151200·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151217·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
CareFusion D.R. 203 Ltd.
FDA registration
CareFusion D.R. 203 Ltd.·1 product·🇩🇴 Dominican Republic
STERIPACK MEDICAL POLAND SP. Z O.O.
FDA registration
STERIPACK MEDICAL POLAND SP. Z O.O.·1 product·🇵🇱 Poland
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408957·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408902·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408940·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408933·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408919·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408926·
TEMPUS 2000 PATIENT MONITOR, MODEL 00-0001; TEMPUS MONITORING STATION, MODEL 01-0011
FDA 510(k)
FDA Class 2
·Cardiovascular
MOBILE-PATIENT VIEWER
FDA 510(k)
FDA Class 2
·Cardiovascular
Agent, Tooth Bonding, Resin
FDA classification
FDA Class 2
·Agent, Tooth Bonding, Resin