6,121 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·TELECTRONICS PASAR MODEL 4171 PG
Microspheres Radionuclide
FDA Pre-Market Approval
FDA Class 3
·TheraSphere
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH(R)II MODELS 262-16
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH(R) II IMPLANT. PACEMAKER PULSE GENERATOR
Microspheres Radionuclide
FDA Pre-Market Approval
FDA Class 3
·SIR-SPHERES MICROSPHERES
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·CYBERTACH(TM) 60 PULSE GENERATOR & PROGRAMMER
Microspheres Radionuclide
FDA Pre-Market Approval
FDA Class 3
·TheraSphere
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·TELECTRONICS PASAR MODEL 4171 PG
Microspheres Radionuclide
FDA Pre-Market Approval
FDA Class 3
·SIR-SPHERES
System, Test, Her-2/Neu, Ihc
FDA Pre-Market Approval
FDA Class 3
·PATHWAY ANTI-HER-2/NEW (4B5)RABBIT MONOCLONAL PRIMARY ANTIBODY
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
FDA Pre-Market Approval
FDA Class 3
·CONSERVE PLUS HIP RESURFACING SYSTEM NEW ENROLLMENT STUDY (NES) PROTOCOL
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·TARGIS TARGETED TRANSURETHRAL THERMOABLATION SYSTEM (TARGIS SYSTEM): NEW POUCH SEALER
VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)
FDA 510(k)
FDA Class 3
·Cardiovascular
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ONE-PIECE ANTERIOR CHAMBER INTRAOCULAR LENSES MODEL 121UV NEW LENS CARRIER
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·ONE-PIECE ANTERIOR CHAMBER INTRAOCULAR LENSES MODEL 121UV NEW LENS CARRIER
ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE
FDA 510(k)
FDA Class 3
·Cardiovascular
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) TOTAL KNEE SYSTEM-ADDITION OF THREE PEGGED PATTELLA PROSTHESES
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·LIVEWIRE TC CARDIAC ABLATION SYSTEM-CABLE 10X ETO REUSE/RESTERILIZATION, NEW EXTENSION CABLE
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) TOTAL KNEE SYSTEM-ADDITION OF THREE PEGGED PATTELLA PROSTHESES
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·NEW JERSEY LCS(R) TOTAL KNEE SYSTEM-ADDITION OF THREE PEGGED PATTELLA PROSTHESES