31 results
·
22ms
·
Sources: EU EUDAMED, US FDA
AFFINITY CP CENTRIFUGAL PUMP, RESTING HEART SYS.,MYOTHERM CARDIOPLEGIA DELIV.,AFFINITY HOLLOW FIBER OXYGENATOR,AAF
FDA 510(k)
FDA Class 2
·Cardiovascular
MAXCUT CARBIDE BUR (100/pk) RA 2
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77811119721·MAXCUT CARBIDE BUR (100/pk) Shape: Round; Size:...
SOLARIS REUSABLE AND DISPOSABLE BLOOD PRESSURE CUFFS
FDA 510(k)
FDA Class 2
·Cardiovascular
DIRECT BILIRUBIN REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
GMK-HINGE 02.09.0312H FIXED TIBIAL INSERT SIZE 3/12MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KRO·December 14, 2022
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 29, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·June 11, 2014
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 2, 2011
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·April 30, 2013
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 15, 2008
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 25, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 25, 2018
NeuraGen Nerve Guide NeuraGen Nerve Guide is indicated for repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.
FDA Enforcement
Class II
·Terminated·Integra LifeSciences Corporation·May 22, 2013
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2017
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NKB·May 6, 2022
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NKB·May 6, 2022
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2017
CD HORIZON - CHROMALOY PLUS ROD
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·July 4, 2025
VITEK® 2 AST-ST01 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LON·October 24, 2017