10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORTHOFUSER WOUND DRAINAGE/AUTOTRANSFUSION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
ENDO-SCRUB®
FDA UDI
MEDTRONIC XOMED, INC.·20681490697785·SHEATH 1912019 5PK 4MM/25 DEG WOLF
"2.0" SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036053444·
BALFOUR MALLEABLE BLADE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896011410·BALFOUR MALLEABLE BLADE WITH PROTECTIVE EDGE
COLOR BUFFED (CB) DDH FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
BENCOX ID STEM, BENCOX METAL HEAD, BENCOX BIPOLAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
STARR-EDWARDS SILASTIC BALL HEART VALVE PROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWQ·October 31, 2019
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·January 11, 2013
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·December 1, 2010
2520274-2014-01026
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code FZX·July 3, 2014