1,071 results · 25ms · Sources: EU EUDAMED, 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