67 results · 64ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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