8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
AESUCLAP SOCON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
artegral
FDA UDI
Merz Dental GmbH·D7091970285·anteriors; shade C1; mould UBM
LIFE SPINE ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AED Sinuscope
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
DEVILBISS
FDA Adverse Event
Injury
·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JGS·February 20, 2013
STRATA II, ADJUSTABLE DELTA VALVE, SMALL
FDA Adverse Event
Injury
·MEDTRONIC NEUROSURGERY·Product code JXG·January 14, 2011
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 31, 2014