10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CONNEX GASTROINTESTINAL SUTURE ANCHOR, MODEL GIAS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VITROS
FDA UDI
ORTHO CLINICAL DIAGNOSTICS·10758750008384·VITROS Immunodiagnostic Products
LH Calibrators
LumaFlex Double J stent, 2 open tips, Ch/Fr7/L.24cm, without wire
FDA UDI
Promepla·03700512967545·
POLYROX 45 JBP
FDA Adverse Event
Other
·BIOTRONIK GMBH AND CO.·Product code DTB·July 17, 2006
MENICON Z
FDA 510(k)
FDA Class 2
·Ophthalmic
VERSALUX
FDA 510(k)
FDA Class 2
·Dental
UNKNOWN LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 19, 2013
ILAB ULTRASOUND IMAGING SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (CE)·Product code OBJ·September 15, 2014
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·May 5, 2011