666 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Dia-Proseal
FDA 510(k)
FDA Class 2
·Dental
OsteoMed
FDA UDI
OSTEOMED LLC·00842528128862·2.0mm x 9mm Cannulated Lag Screw
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100950·DESMARRES LID RETRACTOR #0
HSINER NEBULIZER BOTTLE, CPR MASKS AND FACE SHIELDS
FDA 510(k)
FDA Class 2
·Anesthesiology
AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER
FDA 510(k)
FDA Class 2
·Radiology
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818675·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818682·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818705·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818668·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818651·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818699·
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 10, 2009
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·August 28, 2009
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 18, 2009
EEA 25MM SINGLE-USE STAPLER
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GDW·September 21, 2009
UNK
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·November 18, 2009
ENDO GIA UNIVERSAL 12MM SINGLE USE INST
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GDW·August 19, 2009
GE OEC 9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 18, 2009
EEA 31MM SINGLE-USE STAPLER
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GDW·September 21, 2009
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 21, 2013