25 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RANDOX HUMAN ASSSAYED DRUG CONTROL
FDA 510(k)
FDA Class 1
·Clinical Toxicology
Zirlux
FDA UDI
HENRY SCHEIN, INC.·00304040056202·Zirlux Multi Anterior A2,98.5X18
"2.0MM" SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036008970·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106882·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106868·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106943·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106936·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106967·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106905·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106875·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106950·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106851·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106929·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106912·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304106899·
STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX
FDA 510(k)
FDA Class 2
·Orthopedic
PURILENS SALINE SOLUTION
FDA 510(k)
FDA Class 2
·Ophthalmic
BATTERY 14.8V, 6.3 AH LI-ION BATTERY
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 15, 2013
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·March 9, 2011
UNKNOWN DEPUY INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 11, 2008