77 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MICROLIFE AUTOMATIC TALKING BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
MAKO SURGICAL CORP.·00848486001360·KNEE FEMORAL CHECKPOINT
Bone cutters
FDA UDI
DFS - DIAMON GmbH·04057176148131·Bone Cutter type 165 HP
Flexitron
FDA UDI
Nucletron B.V.·08717213026452·Flexitron Transfer Tube CT/MR for channel 3 (2)
SYNGO NEURO PBV-IR
FDA 510(k)
FDA Class 2
·Radiology
BODY FAT ANALYZER, MODEL HBF-306
FDA 510(k)
FDA Class 2
·Cardiovascular
TruFit™
FDA UDI
Ortho Organizers, Inc.·00190707110185·TruFit™2.0 .018 R UR6 CONV TBT HG-OCC -10T 10DO...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730033925·TruFit™2.0 .018 R UR6 CONV TBT HG-OCC -10T 10DO...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730033154·TruFit™2.0 .018 R UR6 CONV TBT HG-OCC -10T 10DO...
UNKNOWN KNEE FEMORAL ADAPTOR BOLT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019
PLUM A + DRIVER REFU
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 7, 2013
FLEXICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·June 2, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code NIQ·August 11, 2008
TruFit™
FDA UDI
Ortho Organizers, Inc.·00190707160050·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...
TruFit™
FDA UDI
Ortho Organizers, Inc.·00190707160135·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730054050·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730053848·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...
TruFit™
FDA UDI
Ortho Organizers, Inc.·00190707159900·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730054005·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730053930·TruFit™ 2.0 ASM .018 ROTH UR6 CONV TBT -10T 10D...