176 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
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