12 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Leksell Stereotactic System
FDA UDI
Elekta Solutions AB·07340201502495·Insulated Curved Post
Myo/Wire II
FDA UDI
A & E MEDICAL CORPORATION·10841291101727·SS Suture, 4 per sleeve
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450144206·
BD VACUTAINER SINGLE USE NON-STACKABLE HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 6, 2021
MCC-MIV ONE 2 ONE SOFTWARE
FDA 510(k)
FDA Class 2
·Physical Medicine
ACCU-CHEK COMPLETE METER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SEE H10 NARRATIVE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·September 11, 2017
UNKNOWN LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·April 3, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 15, 2011
SILICONE ADVANCED OPTIC-VIOLET SHIELD
FDA Adverse Event
Malfunction
·BAUSCH & LOMB·Product code HQL·May 7, 2008