33 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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IMMULITE/IMMULITE 1000 OM-MA, IMMULITE 2000 OM-MA
FDA 510(k)
FDA Class 2
·Immunology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694020275·FPS 3.5mm x 10mm Standard Screw
Liofilchem MIC Test Strip (MTS)
FDA UDI
LIOFILCHEM SRL·08055182873326·MIC Test Strip is a quantitative assay for dete...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111111006·WANGENSTEEN NH SERR 10 1/2" TC
Vu a-POD™
FDA UDI
Seaspine Orthopedics Corporation·10889981038199·35x27mm Trial 10mm 12 deg. The Vu a-POD interve...
Votion®
FDA UDI
Ortho Organizers, Inc.·00190707113513·Votion .018 MC LR5 HK -17T 2A 0O (10PK) VOTION
Votion
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730007827·Votion 018 MC LR5 HK -17T 2A 0O (10PK)
POINT 4 MODIFIED
FDA 510(k)
FDA Class 2
·Dental
EVOLUTION COLONIC STENT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OsteoMed
FDA UDI
OSTEOMED LLC·00845694074261·FPS 3.5 x 10mm Screw Sterile Qty 2
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020870·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020849·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020764·
InFill V2 Lateral PE
FDA UDI
PINNACLE SPINE GROUP, LLC·00814729020801·
EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MQR·April 12, 2018
ACCU-CHEK TENDER INFUSION SET
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·October 27, 2008
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·August 16, 2011
PIN PULLER
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·July 9, 2013
EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code MQR·August 17, 2017
EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FAD·March 12, 2015