24 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Electro Flo 6 Airway Clearance System
FDA 510(k)
FDA Class 2
·Anesthesiology
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003912·270 micron Holmium Laser Fiber Cable, Single Us...
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113561·IMPLANT BLADE 6.2MM (BX/5)
ZAVATION TAP
FDA UDI
Zavation LLC·00197157021498·MIS Tap 9.0MM
HARDYDISK CEFONICID, 30 MCG
FDA 510(k)
FDA Class 2
·Microbiology
REEVUE INDIRECT CALORIMETER, MODEL#8100
FDA 510(k)
FDA Class 2
·Anesthesiology
UNK SERI SURGICAL SCAFFOLD
FDA Adverse Event
Injury
·ALLERGAN·Product code OXF·June 25, 2014
ARROWG+ARD CATHETER PRODUCTS
FDA Adverse Event
Injury
·ARROW INTL INC·Product code DQO·October 17, 2008
VASOVIEW HEMOPRO EVH SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·August 4, 2011
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP (OUS)
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·June 28, 2013
PROMUS PREMIER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·March 11, 2026
CELL-DYN SAPPHIRE ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·January 30, 2014
PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·May 22, 2014
UNKNOWN KNEE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·March 3, 2016
EDWARDS UNKNOWN SAPIEN TRANSCATHETER HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019
EDWARDS INTRODUCER SET UNKNOWN
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019
EDWARDS UNKNOWN SAPIEN TRANSCATHETER HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019
EDWARDS UNKNOWN SAPIEN TRANSCATHETER HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019
UNKNOWN KNEE TIBIAL INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 23, 2019
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 27, 2011