25 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SOUNDSTAR ECO DIAGNOSTIC ULTRASOUND CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·June 6, 2018
N/A
FDA UDI
MEDTRONIC XOMED, INC.·00763000034658·PROSTHESIS 1112050 H/A TOTAL 75 RECT
NA
FDA UDI
MEDTRONIC XOMED, INC.·00681490033305·PROSTHESIS 1112050 H/A TOTAL 75 RECT
Medline-Microtek
FDA UDI
Microtek Medical LLC·00748426141982·Laser Articulating Arm Drape, 23 cm x 152 cm
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756615044·Arm Sling
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741120500·
MEGA PLUS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809155857208·Rod, Ø6.0 x 500mm
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756974127·Arm Sling
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521112050D0·12 x 50 mm Anodized SI Implant Fully Threaded
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674112050060·
VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Q-SWITCHED ND:YAG LASER SYSTEM, MODEL GLOBALCURE-SC6
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code KWI·January 25, 2017
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 14, 2013
CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL EASE PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 2, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 15, 2008
M2A MODULAR HEAD COMPONENT 38MM HEAD DIAMETER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 19, 2016
8MM TI STRAIGHT RADIAL STEM 28MM-STERILE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWI·January 24, 2017
22MM COCR RADIAL HEAD STANDARD HEIGHT/12.5MM-STERILE
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWI·January 24, 2017