173 results
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16ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SENSAR 3PC & 1PC MONOFOCAL; TECNIS 1PC MONOFOCAL, 1PC MULTIFOCAL AND 1PC TORIC MONOFOCAL, 1PC OPTIBULE & 3PC OPTIBLUE
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STAAR SURGICAL COLLAMER UV-ABSORBING POSTERIOR CHAMBER 1-PC AND 3-PC INTRAOCULAR LENSES
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC . KAPPA 400 SERIES PULSE GENERATORS
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·TECNIS 3PC MULTIFOCAL
Diagnostic Low Electric Field
FDA Pre-Market Approval
FDA Class 3
·MARGINPROBE SYSTEM
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·REZOOM 3-PC MULTIFOCAL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·TENIS 3-PC MONOFOCAL-ZA9003
Test, Urea Adult And Pediatric (Breath),
FDA Pre-Market Approval
FDA Class 3
·PyloPlus UBT System
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·COBAS HPC TEST,240 TESTS AND COBAS HPV TEST, 960 TESTS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·TECNIS® Foldable Acrylic IOL with OptiEdge, Model ZA9003
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·TECNIS® Multifocal 3-Piece IOL, Model ZMA00
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SENSAR® Soft Acrylic Posterior Chamber IOL
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·TECNIS 1-Piece IOL with TECNIS® iTEC Preloaded Delivery System Model PCB00, TECNIS Multifocal 1-PC IOL with TECNIS® iTEC
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·8 ECTRAPROBE-PLR MODEL 900 OPTILASE CONTACT LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·ETHYLENE OXIDE (EO)STERILIZATION EQUIPMENT
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·SPECTRANECTICS CVX-300 EXCIMER LASER SYSTEM
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·Philips Laser System
Stimulator, Autonomic Nerve, Implanted For Stroke Rehabilitation
FDA Pre-Market Approval
FDA Class 3
·Vivistim® System
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·SPECTRAPROBE-PLR CATH. & OPTILASE/CARDIOLASE LASER
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·SPECTRANECTICS CVX-300 EXCIMER LASER SYSTEM