176 results · 18ms · Sources: EU EUDAMED, US FDA

Intracranial Coil-Assist Stent

FDA classification
FDA Class 3 ·Intracranial Coil-Assist Stent

Stent Graft, Bypass, Superficial Femoral Artery

FDA classification
FDA Class 3 ·Stent Graft, Bypass, Superficial Femoral Artery

Scaffold, Dissection Repair

FDA classification
FDA Class 3 ·Scaffold, Dissection Repair

Stent Graft, Infrapopliteal, Venous Arterialization

FDA classification
FDA Class 3 ·Stent Graft, Infrapopliteal, Venous Arterialization

Stent, Iliac Vein

FDA classification
FDA Class 3 ·Stent, Iliac Vein

Transcatheter Septal Occluder (Ventricular)

FDA classification
FDA Class 3 ·Transcatheter Septal Occluder (Ventricular)

Intraocular, Pressure Measuring Device

FDA classification
FDA Class 3 ·Intraocular, Pressure Measuring Device

Transcatheter Septal Occluder (Atrial)

FDA classification
FDA Class 3 ·Transcatheter Septal Occluder (Atrial)

Optical Diagnostic Device For Melanoma Detection

FDA classification
FDA Class 3 ·Optical Diagnostic Device For Melanoma Detection

Aspiration Therapy System

FDA classification
FDA Class 3 ·Aspiration Therapy System

Sensor, Electro-Optical (For Cervical Cancer)

FDA classification
FDA Class 3 ·Sensor, Electro-Optical (For Cervical Cancer)

Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief

FDA classification
FDA Class 3 ·Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief

Stent, Urethral, Prostatic, Semi-Permanent

FDA classification
FDA Class 3 ·Stent, Urethral, Prostatic, Semi-Permanent

Pulse Generator, Permanent, Implantable

FDA classification
FDA Class 3 ·Pulse Generator, Permanent, Implantable

Ophthalmic Sealant

FDA classification
FDA Class 3 ·Ophthalmic Sealant

Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant

FDA classification
FDA Class 3 ·Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant

Gastric Emptying Breath Test

FDA classification
FDA Class 3 ·Gastric Emptying Breath Test

Intrasaccular Flow Disruption Device

FDA classification
FDA Class 3 ·Intrasaccular Flow Disruption Device

Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia

FDA classification
FDA Class 3 ·Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia

Bone, Heterograft

FDA classification
FDA Class 3 ·Bone, Heterograft