11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VARIOUS SURGICAL OR PATIENT DRAPES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PerCP/Cyanine5.5 anti-human CD20
FDA UDI
BIOLEGEND, INC.·00810034701459·URL: https://www.biolegend.com/en-us/products/p...
ZMR®
FDA UDI
Zimmer, Inc.·00889024364769·
ZMR®
FDA UDI
Zimmer, Inc.·00889024364745·
ZMR®
FDA UDI
Zimmer, Inc.·00889024364752·
PRO QR ADVANCED FORMULA POWDER
FDA 510(k)
FDA Unclassified
·Unknown
CREO® Stabilization System
FDA 510(k)
FDA Class 2
·Orthopedic
microlife
FDA UDI
MICROLIFE USA, INC.·06970388160075·
RADIALSOURCE TRANSRADIAL ACCESS KIT
FDA Adverse Event
Malfunction
·GREATBATCH MEDICAL·Product code DYB·June 5, 2014
CURLIN INFUSION IV PUMP
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code FRN·February 1, 2013
JUVEDERM ULTRA XC TSK US
FDA Adverse Event
Injury
·ALLERGAN·Product code LMH·February 1, 2011