132 results · 54ms · Sources: EU EUDAMED, US FDA

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STREAMLINE

FDA Adverse Event
Malfunction ·MENLO CARE, INC.·Product code DQO·August 30, 1996

CENTERMARK PERIPHERALLY INSERTED CENTRAL CATHETER W/17G

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·September 13, 1996

STREAMLINE MIDLINE CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·August 14, 1996

MIDLINE CATHETER

FDA Adverse Event
MENLO CARE, INC.·Product code FOZ·July 16, 1996

LANDMARK MIDLINE CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·July 8, 1996

LANDMARK MIDLINE CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·September 3, 1996

CENTERMARK PERIPHERALLY INSERTED CENTRAL CATHETER

FDA Adverse Event
MENLO CARE, INC.·Product code DQO·August 30, 1996

LANDMARK MIDLINE CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·July 24, 1996

CENTERMARK PERIPHERLLY INSERTED CENTRAL CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code DQO·September 13, 1996

LANDMARK MIDLINE

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·September 19, 1996

CENTERMARK PERIPHERALLY INSERTED CENTRAL

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code DQO·September 13, 1996

LANDMARK

FDA Adverse Event
Other ·MENLO CARE, INC.·Product code FOZ·September 24, 1996

STREAMLINE VASCULAR ACCESS DEVICE

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·July 24, 1996

LANDMARK MIDLINE VENOUS ACCESS DEVICE

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code DQO·August 30, 1996

LANDMARK MIDLINE CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·July 3, 1996

LANDMARK MIDLINE CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code FOZ·September 9, 1996

CENTERMARK CATHETER

FDA Adverse Event
Other ·MENLO CARE, INC.·Product code DQO·September 6, 1996

LANDMARK MIDLINE CATHETER (20 GAUGE)

FDA Adverse Event
Injury ·MENLO CARE INC.·Product code FOZ·August 21, 1996

CENTERMARK PERIPHERALLY INSERTED CENTRAL CATHETER/EXACT CODE

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code DQO·September 27, 1996

CENTERMARK CATHETER

FDA Adverse Event
Injury ·MENLO CARE, INC.·Product code DQO·July 16, 1996