33 results
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20ms
·
Sources: EU EUDAMED, US FDA
CELLTRACKS ANALYZER II
FDA 510(k)
FDA Class 2
·Immunology
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074156002·CASE 7060110 CDHL 6.35 APICAL OUTER
Masel
FDA UDI
Ortho Organizers, Inc.·00190707045906·ADAMS CLASPS SIZE 10MM
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037311943·REAMER Ø10 mm / HUDSON
Claymount
FDA UDI
Varex Imaging Nederland B.V.·08718755000726·x-ray beam-limiting device, to restrict the dim...
Claymount
FDA UDI
Varex Imaging Nederland B.V.·08718755000702·x-ray beam-limiting device, to restrict the dim...
Claymount
FDA UDI
Varex Imaging Nederland B.V.·08718755000719·x-ray beam-limiting device, to restrict the dim...
Canaveral®
FDA UDI
FLOSPINE LLC·B183120601100·6.0mm Curved Rod, Ti Alloy 110mm
MODIFICATION TO TRELEX MESH SURGICAL MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POWDER-FREE NITRILE EXAMINATION GLOVES, WHITE
FDA 510(k)
FDA Class 1
·General Hospital
Widex
FDA UDI
Widex A/S·05706069673166·Widex EVOKE E-CIC (Dark brown ) 110, Right, RC ...
Widex
FDA UDI
Widex A/S·05706069673142·Widex EVOKE E-CIC (Light beige ) 110, Right, RC...
Widex
FDA UDI
Widex A/S·05706069673159·Widex EVOKE E-CIC (Clay brown ) 110, Right, RC ...
MARYLAND BIPOLAR FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·December 20, 2012
IMPELLA CP
FDA Adverse Event
Death
·ABIOMED, INC.·Product code OZD·December 8, 2025
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 5, 2013
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 15, 2011
SOFT TOUCH II
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·June 10, 2008
EMBLEM MRI S-ICD
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 12, 2023
PROGRASP FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 30, 2013