10,000 results
·
47ms
·
Sources: EU EUDAMED, US FDA
Biomet®
FDA UDI
Biomet Orthopedics, LLC·00887868483387·
Vanguard 360 Revision System
FDA UDI
Biomet Orthopedics, LLC·00880304482425·
BIOMET 360 KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304481725·
BIOMET KNEE STEM EXTENSION TRIAL
FDA UDI
Biomet Orthopedics, LLC·00880304324589·
VANGUARD 360
FDA UDI
Biomet Orthopedics, LLC·00880304501898·
VANGUARD INSTRUMENT
FDA UDI
Biomet Orthopedics, LLC·00880304515796·
VANGUARD 360 INSTRUMENT
FDA UDI
Biomet Orthopedics, LLC·00880304531826·
Vanguard® Instrument
FDA UDI
Biomet Orthopedics, LLC·00887868563591·
VANGUARD 360
FDA UDI
Biomet Orthopedics, LLC·00880304501348·
Vanguard® 360 Instrument
FDA UDI
Biomet Orthopedics, LLC·00887868563799·
Biomet® 360 Instrument
FDA UDI
Biomet Orthopedics, LLC·00887868562273·
BIOMET KNEE
FDA UDI
Biomet Orthopedics, LLC·00880304011397·
VANGUARD 360
FDA UDI
Biomet Orthopedics, LLC·00880304502154·
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·KAPPA 600/700/650/800/900/SIGMA/MEDTRONIC 350 IPG/ENPULSE/ADAPTA/VERSIA/SENSIA/RELIA FAMILIES OF IPG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REVO MRI SURESCAN IPG AND PACING SYSTEM
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Genesis and EON Family Neurostimulation (IPG) System
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CAPSURE FIX LEAD & REVO MRI IPG
Stimulator, Hypoglossal Nerve, Implanted, Apnea
FDA Pre-Market Approval
FDA Class 3
·Inspire Model 3028 Implantable Pulse Generator (IPG)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CAPSURE FIX LEAD & REVO MRI IPG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CAPSUREFIX MRI LEAD, REVO MRI SURESCAN IPG