4,599 results · 44ms · Sources: EU EUDAMED, US FDA

Hys. 027.00.3020a 40k

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

Hys. 020.00.3020a 40k

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

Hys. 020.00.2600a 40k

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

Hys. 020.00.1875a 40k

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Blazejewski MEDI-TECH GmbH·1 device

Intraocular Lens

FDA Pre-Market Approval
FDA Class 3 ·TECNIS Symfony Toric Extended Range of Vision IOLs

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·PRESTIGE LP Cervical Disc

Intraocular Pressure Lowering Implant

FDA Pre-Market Approval
FDA Class 3 ·iStent inject Trabecular Micro-Bypass System

Stimulator, Hypoglossal Nerve, Implanted, Apnea

FDA Pre-Market Approval
FDA Class 3 ·Inspire II Upper Airway Stimulator

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·iDESIGN Refractive Studio and STAR S4 IR Excimer Laser Systems

Intracranial Coil-Assist Stent

FDA Pre-Market Approval
FDA Class 3 ·Neuroform Atlas® Stent System

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·M6-C Artificial Cervical Disc

Mr-Guided Focused Ultrasound System

FDA Pre-Market Approval
FDA Class 3 ·ExAblate Neuro Thalamotomy

Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled

FDA Pre-Market Approval
FDA Class 3 ·NATRELLE Highly Cohesive Anatomically Shaped Silicone-Filled Breast Implants

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval
FDA Class 3 ·MANAGE HF Study

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·CentriMag Circulatory Support System

Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia

FDA Pre-Market Approval
FDA Class 3 ·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear

Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·ORSIRO Sirolimus Eluting Coronary Stent System

Stent, Iliac Vein

FDA Pre-Market Approval
FDA Class 3 ·VICI VENOUS STENT System

Stimulator, Hypoglossal Nerve, Implanted, Apnea

FDA Pre-Market Approval
FDA Class 3 ·Inspire II Upper Airway Stimulator

Reherniation Reduction Device

FDA Pre-Market Approval
FDA Class 3 ·Barricaid Annular Closure Device