50 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NEXSTAT PLUS AND NEXFOAM PLUS TOPICAL HEMOSTAT DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
Simpliciti™
FDA UDI
TORNIER, INC.·00846832061365·
Tornier Simpliciti® Shoulder System
FDA UDI
TORNIER, INC.·00846832091881·
METATARSOPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CD HORIZON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 21, 2013
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·September 26, 2014
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·June 14, 2011
TARGET DEVICE 300X160MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·March 2, 2012
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORP.·Product code OKS·August 19, 2014
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·January 13, 2017
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·January 5, 2017
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016
LACRIFAST
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code OKS·December 25, 2016