332 results · 80ms · Sources: EU EUDAMED, US FDA

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Pre-lubricated urinary catheter

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Lentismed d.o.o.·21 devices

ULTRA CATHETER

FDA Adverse Event
Injury ·CURE MEDICAL LLC·Product code KOD·March 3, 2020

L3C0600 - CURE PRODUCTS

FDA Adverse Event
Injury ·CONVATEC INC·Product code EZD·March 1, 2022

L3C0600 - CURE PRODUCTS

FDA Adverse Event
Injury ·CONVATEC INC·Product code EZD·March 2, 2022

CURE MALE ULTRA

FDA Adverse Event
Injury ·CURE MEDICAL LLC·Product code KOD·January 28, 2020

SURESTEP¿ FOLEY TRAY SYSTEM BARDEX® ALL- SILICONE FOLEY CATHETER TRAY

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·February 13, 2019

SURESTEP¿ FOLEY TRAY SYSTEM BARDEX® IC COMPLETE CARE®

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·November 10, 2022

TWIST CATHETER

FDA Adverse Event
Injury ·CURE MEDICAL LLC·Product code KOD·January 15, 2021

BARDIA URETHRAL CATHETER

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·December 11, 2020

1018233-2019-01468

FDA Adverse Event
Injury ·March 20, 2019

BARD TOUCHLESS PLUS UNISEX PRE-LUBRICATED RUBBER URETHRAL CATHETER KIT

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·September 14, 2020

BARD TOUCHLESS PLUS UNISEX PRE-LUBRICATED VINYL URETHRAL CATHETER KIT

FDA Adverse Event
Malfunction ·C. R. BARD, INC.·Product code FCM·October 4, 2023

BARD® TOUCHLESS® PLUS UNISEX PRE-LUBRICATED VINYL URETHRAL CATHETER KIT

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·October 1, 2018

SURESTEP¿ FOLEY TRAY SYSTEM BARDEX® IC COMPLETE CARE®

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·September 5, 2023

ULTRA CATHETER

FDA Adverse Event
Injury ·CURE MEDICAL LLC·Product code KOD·May 28, 2021

MAGIC3 GO MALE COUDE CATHETER WITH SUREGRIP

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZD·October 21, 2022

BARD® URETHRAL CATHETERIZATION TRAY WITH RED RUBBER CATHETER

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOD·January 4, 2019

INTERMITTENT CATHETER

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GBM·August 22, 2022

BARDEX® ALL-SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZL·March 20, 2024

BARDEX® ALL-SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code EZL·March 21, 2023