14 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ESOPHYX2 HD
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ESOPHYX Z
FDA Adverse Event
Injury
·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550124·GENUMEDI PT KNEE SUP SILVER L EW III
LACTOSORB* 2.0MM SYSTEM TEMPLATE
FDA UDI
BIOMET MICROFIXATION, INC·00888233011983·
LACTOSORB* 2.0MM SYSTEM TEMPLATE
FDA UDI
BIOMET MICROFIXATION, INC·00841036130763·
SELMAN TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896024052·SELMAN TISSUE FORCEPS ROUND CUP TEETH
GE VENUE 40 COMPACT DIAGNOSTIC ULTRASOUND
FDA 510(k)
FDA Class 2
·Radiology
ZOE FLUID STATUS MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
ONE TOUCH ULTRA MINI TEST STRIPS
FDA Adverse Event
Injury
·Product code CGA·May 15, 2014
OCTRODE
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 28, 2013
EON IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 25, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 4, 2014
TECNIS SIMPLICITY
FDA Adverse Event
Injury
·AMO PUERTO RICO MFG. INC.·Product code HQL·February 7, 2023
BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.
FDA Recall
Terminated
·Becton Dickinson & Company·Product code FPA·February 19, 2015