443 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL DEVICES
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL ES DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Tissue Graft Of 6mm And Greater
FDA Pre-Market Approval
FDA Class 3
·BIOPOLYMERIC(TM) VASCULAR GRAFT
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL VHD
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (VASCULAR HEMOSTASIS DEVICE)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL 4-5 FRENCH SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS(R) MODEL 6001,3,33 DDD MODEL CPRI MODEL P2A
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Drug-Coated Peripheral Transluminal Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·Lutonix 018 Drug Coated Balloon PTA Catheter (Lutonix DCB)
Drug-Eluting Peripheral Transluminal Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·Lutonix 035 Drug Coated Balloon PTA Catheter (Lutonix DCB)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Drug-Eluting Peripheral Transluminal Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·Lutonix 018 Drug Coated Balloon PTA Catheter (Lutonix DCB)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS(R) MODEL 6001,3,33 DDD MODEL CPRI MODEL P2A
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AURORA MODELS 6291 & 6292 MULTIPROGRAM. DDD P. GEN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CHORUS(R) MODEL 6004&6034 DDD MODEL CPRI MODEL P2A