49 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AESKUSLIDES ANA HEP-2
FDA 510(k)
FDA Class 2
·Immunology
ArgenPMMA 98x25-A1
FDA UDI
ARGEN CORPORATION, THE·D818120889·Crown And Bridge, Temporary, Resin
Mini Unicycle™
FDA UDI
Ortho Organizers, Inc.·00190707056902·Mini Unicycle™ .120” Ligature Ties - Teal
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450254608·
ENDOSKELETON TC
FDA 510(k)
FDA Class 2
·Orthopedic
ENDOSCOPIC LIGHT SOURCE XL202/L3
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
2520274-2013-02684
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·May 20, 2013
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 12, 2011
CONTOUR CURVED CUTTER STAPLER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC·Product code GDW·August 18, 2008
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