628 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ProgenaMatrix
FDA 510(k)
FDA Unclassified
·Unknown
Monoject
FDA UDI
Cardinal Health 200, LLC·10192253024982·Hypodermic Safety Needle 20G x 1" (0.9 x 25 mm)
Monoject
FDA UDI
Cardinal Health, Inc.·10884521544604·Hypodermic Safety Needle
FX V 135 stem
FDA UDI
FX SOLUTIONS·03701037318478·FX V135 LONG STEM TA6V CEMENTLESS Ø32/08 LG200m...
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127384·2.0 X 10mm Cannulated Headed Screw, T7
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab
SCANLAN® MicroSurgical Instruments
FDA UDI
SCANLAN INTERNATIONAL INC·00846159027907·Joseph Double Hook
VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET
FDA 510(k)
FDA Class 2
·General Hospital
STRYKER DISPOSABLE CRANIAL PERFORATOR BIT
FDA 510(k)
FDA Class 2
·Neurology
NA
FDA UDI
STRYKER CORPORATION·04546540939852·2108 Series Sagittal Blade, Ground (19.1 x 1.32...
ARI Anterior Staple System
FDA UDI
VB Spine LLC·10888857235694·Dual Hole Staple Guide (Right) Size 18 mm
ARI Anterior Staple System
FDA UDI
VB Spine LLC·10888857235670·Dual Hole Staple Guide (Right) Size 13 mm
ARI Anterior Staple System
FDA UDI
VB Spine LLC·10888857235687·Dual Hole Staple Guide (Right) Size 16 mm
HEARTSINE SAMARITAN 300P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·November 16, 2012
DA VINCI SI SURGICAL SYSTEM
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC.·Product code NAY·March 26, 2010
DA VINCI S SURGICAL SYSTEM
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC.·Product code NAY·March 26, 2010
ACRYSOF RESTORE
FDA Adverse Event
Injury
·ALCON RESEARCH. LTD. / HUNTINGTON·Product code MFK·February 18, 2010
BD NEXIVA
FDA Adverse Event
Other
·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·June 18, 2010
ACRYSOF IQ TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·November 3, 2010
ACRYSOF IQ TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 3, 2010