24 results · 34ms · Sources: EU EUDAMED, US FDA

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Cook Silicone Balloon HSG Catheter

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 20, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 30, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 20, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 20, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 22, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 22, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·April 20, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·March 11, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·March 4, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·February 1, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·March 11, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·December 2, 2021

COOK SILICONE BALLOON HYSTEROSALPINGOGRAPHY INJECTION CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LKF·December 2, 2021

Femoral Sizer

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063788·

INTUITIVE SURGICAL DA VINCI ENDOSCOPIC INSTRUMENTS AND CONTROL SYSTEM AND ENDOWRIST STABILIZER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

NAVIAID ICVI-F DEVICE, NAVIAID ICVI-S DEVICE, NAVIAID ICVI-B DEVICE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·September 3, 2021

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 27, 2011

OBTRYX SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013