67 results
·
64ms
·
Sources: EU EUDAMED, US FDA
J-UMIL-050037; UMI-LOC LOCKABLE UTERINE MANIPULATOR INJECTOR
FDA Adverse Event
Injury
·CATHETER RESEARCH, INC.·Product code LKF·August 7, 2015
HS CATHETER, 5F
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code LKF·July 16, 2015
J-UMIL-050037; UMI-LOC LOCKABLE UTERINE MANIPULATOR INJECTOR
FDA Adverse Event
Injury
·CATHETER RESEARCH, INC.·Product code LKF·August 7, 2015
J-UMIL-050037; UMI-LOC LOCKABLE UTERINE MANIPULATOR INJECTOR
FDA Adverse Event
Injury
·CATHETER RESEARCH, INC.·Product code LKF·August 7, 2015
UTERINE MANIPULATOR & INJECTOR (PUMI) 4.5MM
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code LKF·November 17, 2017
CONNECTOR TUBING BX 100
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021
CONNECTOR TUBING BX 100
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021
CONNECTOR TUBING BX 100
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021
CONNECTOR TUBING BX 100
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021
UTERINE MANIPULATOR/INJECTOR
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code LKF·March 13, 2017
CONNECTOR TUBING BX 100
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code DXT·August 13, 2021
ZANNANTI MANIPULATOR
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code LKF·November 28, 2016
ZINNANTI MANIPULATOR
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code LKF·April 21, 2017
PUMI
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC.·Product code LKF·May 1, 2017
UTERINE MANIPULATOR / INJECTOR
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC·Product code LKF·May 3, 2017
HSG Trays/HS 5F Catheter Combo; HSG Procedure Tray+ Shapeable 5F HSG catheter. For hysterosonography and hysterosalpingography, gynecological use.
FDA Recall
Terminated
·Catheter Research, Inc·Product code HGS·April 7, 2015
K-UMI MANIPULATOR, SIZE 5 MM, LENGTH 33CM
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC. (THOMAS MEDICAL)·Product code LKF·September 19, 2024
UTERINE MANIPULATOR
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC. (THOMAS MEDICAL)·Product code LKF·September 28, 2017
Zinnanti Injector - 2.0; Size 2.0 mm, Length 23 cm, latex free, single-use, sterile. For in-office or hospital use when efficient sealing of the uterine cervix is required for the injection of liquid or gas such as hysterosalpingography, salpingoplasties, hydrotubation and Rubin''s test. REF TMI1153.
FDA Recall
Terminated
·Catheter Research, Inc·Product code LKF·April 24, 2006
CANNULA, MANIPULATOR/INJECTOR, UTERINE
FDA Adverse Event
Malfunction
·CATHETER RESEARCH, INC./THOMAS MEDICAL INC.·Product code LKF·September 12, 2017