9 results
·
23ms
·
Sources: EU EUDAMED, US FDA
CEDIA DAU THC CALIBRATORS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515244481·Antrum Grasping Fcps, 90 deg x 120 deg jaws
PERFECTA PDA TOTAL HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SGARLATO FLEXIBLE HINGE TOE IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
LOCKING COND PL 1.5 SHAFT 6HO HE 2HO SST
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·August 13, 2018
NATURALYTE
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 23, 2014
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION INC·Product code DRM·January 2, 2013
SYBRONPRO XRT
FDA Adverse Event
Injury
·EBI INC.·Product code DZE·December 22, 2010
1.5MM LCP CONDYLAR PLATE 6 HOLE SHAFT
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·August 13, 2018