10,000 results
·
55ms
·
Sources: EU EUDAMED, US FDA
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·ZILVER PTX DRUG-ELUTING PERIPHERAL STENT
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·SAULFON PW-70 A&B
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Intraocular Lenses
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVISC Ophthalmic Viscosurgical Device
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVSIC Ophthalmic Viscosurgical Device
Prosthesis, Posterior Spinal Elements
FDA Pre-Market Approval
FDA Class 3
·TOPS System
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReStor Posterior Chamber Intraocular Lenses
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF/ACRYSOF RESTOR/PMMA INTRAOCULAR LENSES
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·THE SUNLIGHT OMNISENSE(TM) ULTRASOUND BONE SONOMETER
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·samaritan Public Access Automated External Defibrillators and Accessories
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·ACRYSOF IQ RESTOR +3.0 D MULTIFOCAL TORIC INTRAOCULAR LENS
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·Zilver Flex(R) 35 Vascular Stent
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·OMNISENSE 7000S ULTRASOUND BONE SONOMETER
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVISC TM VISCOELASTIC PREPARATION
Prosthesis, Posterior Spinal Elements
FDA Pre-Market Approval
FDA Class 3
·TOPS System
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·ZILVER VASCULAR STENT
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·PROVISC Ophthalmic Viscosurgical Device
Mycobacterium Tuberculosis, Cell Mediated Immune Response, Enzyme-Linked Immunospot Test
FDA Pre-Market Approval
FDA Class 3
·T-SPOT .TB TEST
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·samaritan® PAD 350P (SAM 350P), samaritan® PAD 360P (SAM 360P), samaritan® PAD 450P (SAM 450P), Pad-Paks (Adult, Pediatr