24 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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