13 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARTICUL/EZE FEMORAL HEADS
FDA 510(k)
FDA Class 2
·Orthopedic
ARTICULEZE M HEAD 36MM +5 K980513
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 14, 2016
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79805131·Sprint II Bracket McLaugh/Benn/Trev. .018" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79805130051·Sprint II Bracket McLaugh/Benn/Trev. .018" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79805131001·Sprint II Bracket McLaugh/Benn/Trev. .018" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79805130101·Sprint II Bracket McLaugh/Benn/Trev. .018" max....
QLASER SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
CustomizedBone Service
FDA 510(k)
FDA Class 2
·Neurology
ENDOPATH ENDOSCOPIC MULTIFEED STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GAG·February 9, 1998
SILHOUETTE SPINAL FIXATION SYSTEM
FDA Adverse Event
Other
·CENTERPULSE SPINE-TECH, INC.·Product code MCV·November 20, 2003
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·February 22, 2013
UNICEL® DXC 600I SYNCHRON ® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·February 7, 2011
UNKNOWN HIP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·August 5, 2014