8 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NADIA SI Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319705568·Baron Suction Tube 3Fr. (1mm), w/ finger cut-of...
THERMAGE THERMACOOL NXT SYSTEM AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EXSALT WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
M2A MAGNUM PF CUP 66MM O.D. X 60MM I.D.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 26, 2016
ADVANTA
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·October 2, 2008
CURLIN ADMINISTRATION SET
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code FRN·July 27, 2011
DEKNATAL BL MF 0 TC-43 2N 48"
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GAT·June 21, 2013