6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
TUBE TENDER
FDA 510(k)
FDA Class 1
·Cardiovascular
MODIFICATION TO HAKIM PRECISION VALVE SYSTEM, HAKIM PROGRAMMABLE VALVE SYSTEM, HAKIM MICRO PROGRAMMABLE VALVE SYSTEM, SI
FDA 510(k)
FDA Class 2
·Neurology
Gaudi Proximal Humerus Plate
FDA 510(k)
FDA Class 2
·Orthopedic
INTROCAN SAFETY
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FOZ·May 5, 2014
VENUS COMPOSITE
FDA Adverse Event
Injury
·HERAEUS KULZER GMBH·Product code EBF·November 7, 2012
PORTEX BLUE LINE ULTRA 8.00MM TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·September 16, 2010