24 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Columbus Guidewire
FDA 510(k)
FDA Class 2
·Cardiovascular
Olympus
FDA UDI
Gyrus ACMI, LLC·00810008185278·ES-IP EXPANDED IN-ROOM System 25RU with Optiona...
Oph. Cystotomes
FDA UDI
KATENA PRODUCTS, INC.·00841668113738·CCC CYSTOTOME FORMED 25GA
DESS dental smart solutions
FDA UDI
TERRATS MEDICAL SL.·08435457200819·Conic OSS
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964109959·Custom Procedure Kit
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964108624·Custom Procedure Kit
O-arm O2 Imaging System
FDA 510(k)
FDA Class 2
·Radiology
OCULIGHT SL/SLX
FDA 510(k)
FDA Class 2
·Ophthalmic
BD PARADIGM LINK GLUCOSE MONITOR
FDA Adverse Event
Other
·NOVA BIOMEDICAL CORPORATION·Product code NBW·October 10, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
MEDEL S.P.A.·Product code BTI·July 1, 2013
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 26, 2017
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·September 25, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·July 13, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·May 23, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 7, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·November 28, 2024
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·October 31, 2023
ANEURX - UNK
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·May 13, 2016
TALENT AAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·May 13, 2016