356 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DEPUY LPS PROXIMAL TIBIAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040049242·Plier Mathieu Delicate Tip
CD Horizon® ProLock™ Crosslink® Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169578364·TRAY 7062301 PROLOCK IMPLANT TRAY
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496062301·SCOTTISH KNEE-HIGH 100 UNISEX, SIZE XL, MOSTO, ...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111054341·ADULT DUAL STETH 30" BURGUNDY
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981269272·16x14x05mm, 7 Deg w/ Plate
OsteoMed
FDA UDI
OSTEOMED LLC·00845694034630·CFx Two, Base
ECAT2 Generic
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ECAT2010·
IMMULITE 2000 DIGOXIN, MODELS L2KDI2 (200 TESTS) AND L2KDI6 (600 TESTS)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SUPER 12
FDA 510(k)
FDA Class 2
·Dental
SURGISTOOL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FZM·April 16, 2013
UNIVERSAL DRIVER
FDA Adverse Event
Malfunction
·ABBOTT SPINE·Product code HXX·June 18, 2008
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·April 12, 2011
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
CONSULT HCG TEST
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code JHI·March 4, 2025
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026