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