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RENOVORX, INC.

FDA registration
RENOVORX, INC.·1 product·🇺🇸 United States

RenovoCath

FDA UDI
Renovorx, Inc.·00851994005003·The RenovoCath is a multi-lumen, dual-balloon c...

RENOVOCATH RC120

FDA Adverse Event
Injury ·RENOVORX, INC.·Product code MJN·April 13, 2022

RENOVOCATH

FDA Adverse Event
Malfunction ·RENOVORX, INC.·Product code MJN·May 19, 2022

RENOVOCATH

FDA Adverse Event
Malfunction ·RENOVORX, INC.·Product code MJN·April 28, 2022

RENOVOCATH RC120

FDA Adverse Event
Malfunction ·RENOVORX, INC.·Product code MJN·April 13, 2022

RENOVOCATH RC 120

FDA Adverse Event
Injury ·RENOVORX, INC.·Product code MJN·March 29, 2022

RENOVOCATH

FDA Adverse Event
Malfunction ·RENOVORX, INC.·Product code MJN·March 18, 2022

RENOVOCATH

FDA Adverse Event
Malfunction ·RENOVORX, INC.·Product code MJN·March 1, 2022

RENOVOCATH RC 120

FDA Adverse Event
Injury ·RENOVORX, INC.·Product code MJN·March 29, 2022

RENOVOCATH

FDA Adverse Event
Death ·RENOVORX, INC.·Product code MJN·March 29, 2022

RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number: MMRC120-DB-1111; Rx only. Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system.

FDA Recall
Terminated ·RenovoRx, Inc.·Product code MJN·November 25, 2015

RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number: MMRC120-DB-1111; Rx only. Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system.

FDA Enforcement
Class II ·Terminated·RenovoRx, Inc.·January 6, 2016

MPS Medical Product Service GmbH

Authorized representative
🇩🇪 Germany·35 Manufacturers·1959 Devices