1,071 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MALECOT RUSSEL GASTROSTOMY CATHETER
FDA Adverse Event
Other
·COOK, INC.·Product code EZK·October 22, 2003
ULTRATHANE WILLS-OGLESBY SINGLE LUMEN PERCUTANEOUS GASTROSTOMY SET
FDA Adverse Event
Death
·COOK INC·Product code EZK·November 10, 2010
ULTRATHANE WILLS-OGLESBY SINGLE LUMEN PERCUTANEOUS GASTROSTOMY SET
FDA Adverse Event
Malfunction
·COOK, INC.·Product code EZK·June 26, 2009
PYRAMESH
FDA Adverse Event
Injury
·SOFAMOR DANEK MFG.·Product code EZK·September 8, 1998
ULTRATHANE WILLS-OGLESBY SINGLE LUMEN PERCUTANEOUS GASTROSTOMY SET
FDA Adverse Event
Malfunction
·COOK, INC.·Product code EZK·March 11, 2011
MALECOT RUSSEL GASTROSTOMY CATHETER
FDA Adverse Event
Malfunction
·COOK, INC.·Product code EZK·November 11, 2005
WILLS-OGLESBY GASTROSTOMY CATHETER
FDA Adverse Event
Malfunction
·COOK, INC.·Product code EZK·December 13, 2007
UNKNOWN
FDA Adverse Event
Injury
·UNKNOWN·Product code EZK·March 5, 1992
ULTRATHANE WILLS-OGLESBY SINGLE LUMEN PERCUTANEOUS GASTROSTOMY SET
FDA Adverse Event
Injury
·COOK INC.·Product code EZK·January 14, 2009
LUBRI-SIL
FDA Adverse Event
Malfunction
·C.R. BARD, INC.·Product code EZK·September 1, 2016
LUBRI-SIL
FDA Adverse Event
Malfunction
·C.R. BARD, INC.·Product code EZK·September 1, 2016
Catheter, Retention Type
FDA classification
FDA Class 2
·Catheter, Retention Type
REALLOY E.K.
FDA registration
REALLOY E.K.·1 product·🇩🇪 Germany
PANTRAK E.K.
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ETI-EBK PLUS
FDA UDI
DIASORIN SPA·08056771102353·
MeKo Manufacturing e.K.
FDA registration
MeKo Manufacturing e.K.·1 product·🇩🇪 Germany
ETI-AB-EBK PLUS
FDA UDI
DIASORIN SPA·08056771102346·
IONOMETER E-HK AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Hematology
EKS
FDA registration
EKS·2 products·🇭🇰 Hong Kong
JOSEF BETZLER SURGICAL INSTRUMENTS e.K.
FDA registration
JOSEF BETZLER SURGICAL INSTRUMENTS e.K.·13 products·🇩🇪 Germany