31 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EPS320 CARDIAC STIMULATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012475·Zirlux 16+ C1 95X22
INTER FIX™ RP Threaded Fusion Device
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00673978957463·18X26 INTERFIXRP FUSION DEVICE
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780781·LEVAMED ACTIVE ANKLE SUP SLVR L VI
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076659·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076666·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076734·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076680·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076673·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076710·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076741·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076642·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076697·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076703·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304076727·
RAICHEM CREATININE URINE STANDARD
FDA 510(k)
FDA Class 2
·Clinical Chemistry
FORTADERM WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code DHA·March 19, 2013
ACRYSOF
FDA Adverse Event
Other
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·February 25, 2011
COULTER ACT 10
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·March 11, 2008