24 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EVERSTICKNET
FDA 510(k)
FDA Class 2
·Dental
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012260·Zirlux 16+ B4 95X20
SEE H10
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KXA·November 1, 2011
BLAKE DRAIN
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GCY·September 23, 1997
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074402·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074396·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074303·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074310·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074358·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074365·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074341·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074327·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304074334·
COMBOSAFE SURGICAL GOWNS, NON-STERILE (75X REUSABLE)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DC-TELL
FDA 510(k)
FDA Class 2
·Dental
BD MULTITEST¿
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code GKZ·October 8, 2021
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code FNL·March 19, 2013
CONCHA NEPTUNE HEATER
FDA Adverse Event
Other
·TELEFLEX MEDICAL·Product code BZE·February 22, 2011
DURA STAR RX PTCA BALLOON CATHETER
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code LOX·March 11, 2008
GORE® TRI-LOBE BALLOON CATHETER
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DQY·February 24, 2021