916 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GTX 12 GIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
Bur PM2-70 50K Diam Ø1.8x80
FDA UDI
Bien-Air Surgery SA·07630055504258·
Senti Desktop Flex (Basic Set)
FDA UDI
PATH medical GmbH·04260223142987·Senti Desktop Flex Basic Set Content:
1. Case A...
JACOBSON BULLDOG CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921004700·JACOBSON BULLDOG CLAMP STRAIGHT
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450177792·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450177624·
Senti Desktop Flex
FDA UDI
PATH medical GmbH·04260223145285·Senti Desktop Flex Screening Set
Content:
1. Ca...
ZEUS-P
FDA UDI
SPINAL ELEMENTS·00840916153175·Zeus-P Inserter
Stickring Ligature Holder
FDA UDI
TP ORTHODONTICS INC·00192029039113·Stickring Ligature Holder
R & D 4K RETIC
FDA 510(k)
FDA Class 2
·Hematology
UNIPLATE ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SPRINTER LEGEND RX BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code LOX·May 17, 2011
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code NJE·May 8, 2013
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026
LIGASURE
FDA Adverse Event
Injury
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018