28 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ALEUTIAN SPACER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
JOBST SensiFoot
FDA UDI
BSN MEDICAL, INC.·00035664108434·SENSFOOT 8-15 CREW L BR 1 EN FR ES
Leva® Anterior Interbody System
FDA UDI
Spine Wave, Inc.·10840642108880·Plate, 38 mm (W) x 9 mm (H)
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306818981·Carroll Prostatic Retractor w/Simpson Handle, ...
Trial Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964085475·Trial Procedure Kit
ABREU, MODEL 700
FDA 510(k)
FDA Class 2
·General Hospital
DURAMAX CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BD VEO INSULIN SYRINGE WITH THE BD ULTRA-FINE NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·August 27, 2020
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014
PRISMAFLEX
FDA Adverse Event
Death
·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·November 2, 2012
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 15, 2012
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·December 23, 2013
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 9, 2013
SYNCHRON LX 20 PRO CLINICAL SYSTEMS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 2, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 14, 2008
PRISMAFLEX
FDA Adverse Event
Injury
·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014
PRISMAFLEX
FDA Adverse Event
Death
·GAMBRO LUNDIA AB·Product code KDI·January 10, 2014
PRISMAFLEX
FDA Adverse Event
Death
·GAMBRO LUNDIA AB·Product code KDI·January 3, 2014
PRISMAFLEX
FDA Adverse Event
GAMBRO LUNDIA AB·Product code KDI·February 6, 2014