10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GREINER VACUETTE BLOOD COLLECTION TUBE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623294·PEEK Corp Core, Ø12x39mm
TULA Tube Delivery System
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
TOTAL PROTEIN URINE/CSF GEN.3
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ZEPHIR ANTERIOR CERVICAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009
BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
UNIVERSAL KEYLESS DRILL ATTACHMENT 1000 RPM
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL S.A.·Product code GFA·February 1, 2013
SYNCHRON UNICEL DXC 600
FDA Adverse Event
BECKMAN COULTER INC.·Product code JJE·January 26, 2011
7MM TI STRAIGHT RADIAL STEM 26MM-STERILE
FDA Adverse Event
Injury
·SYNTHES USA·Product code KWI·July 31, 2014