12 results
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41ms
·
Sources: EU EUDAMED, US FDA
DLP Suction Tube
FDA registration
Medtronic Mexico S. de R.L. de CV·1 product·🇲🇽 Mexico
DLP Suction Tube
FDA registration
MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States
DLP Suction Tube
FDA registration
Medtronic Grand Rapids·1 product·🇺🇸 United States
Sterigenics US LLC
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
MACRO SUCTION TUBE MODEL NO 10061
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Apparatus, Suction, Single Patient Use, Portable, Nonpowered
FDA classification
FDA Class 1
·Apparatus, Suction, Single Patient Use, Portable, Nonpowered
cmAngio V1.6
FDA registration
CUREMETRIX, INC.·1 product·🇺🇸 United States
ARGOS
FDA registration
santec OIS Corporation·1 product·🇯🇵 Japan
ARGOS
FDA 510(k)
FDA Class 2
·Ophthalmic
PRECIMED CANNULATED SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Device, Analysis, Anterior Segment
FDA classification
FDA Class 2
·Device, Analysis, Anterior Segment
Screw, Fixation, Bone
FDA classification
FDA Class 2
·Screw, Fixation, Bone