13 results
·
27ms
·
Sources: EU EUDAMED, US FDA
CUFFABLE
FDA 510(k)
FDA Class 2
·Cardiovascular
PAQ.112X100X160.BIOCARE
FDA UDI
AB MEDICA GROUP, S.A.·08428763008729·
Couture Essence
FDA UDI
Carolon Company·00078301971237·
Couture Essence
FDA UDI
Carolon Company·00078301911233·
Accu-Beam
FDA UDI
TRANSAMERICAN TECHNOLOGIES INTERNATIONAL·B1779112130·Re-usable fiberoptic handpiece for lasers.
Str...
Maestro®
FDA UDI
Ortho Organizers, Inc.·00190707046774·.018 UR7 NC Std -14T 0A 10DO
VISION ONE LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO SYNCHRON LX 20 CLINICAL CHEMISTRY SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SYNCHRON LX 20 PRO CLINICAL SYSTEMS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 8, 2011
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER INC.·Product code JJE·November 30, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 2, 2014
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·December 14, 2012
BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·July 23, 2020