10,000 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non-CRT)
Agent, Absorbable Hemostatic, Collagen Based
FDA Pre-Market Approval
FDA Class 3
·AVITENE(R) NON-WOVEN WEB
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non- Crt)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non-CRT)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ALL NON-RATE RESPONSIVE PACEMAKERS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non-CRT)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non-CRT)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non-CRT)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Implantable Cardioverter Defibrillator (Non-CRT)
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR SYSTEM & SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM
System, Rf/Microwave Hyperthermia, Cancer Treatment
FDA Pre-Market Approval
FDA Class 3
·BSD-500 HYPERTHERMIA SYSTEM
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft
Stent, Urethral, Prostatic, Semi-Permanent
FDA Pre-Market Approval
FDA Class 3
·THE SPANNER TEMPORARY PROSTATIC STENT
System, Rf/Microwave Hyperthermia, Cancer Treatment
FDA Pre-Market Approval
FDA Class 3
·BSD-500 HYPERTHERMIA SYSTEM
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·AUGMENT BONE GRAFT
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·AUGMENT Bone Graft and AUGMENT Injectable
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·I-FACTOR PEPTIDE ENHANCED BONE GRAFT
Stent, Urethral, Prostatic, Semi-Permanent
FDA Pre-Market Approval
FDA Class 3
·SPANNER TEMPORARY PROSTATIC STENT WITH DISTAL CURVE DESIGN CHANGE
System, Rf/Microwave Hyperthermia, Cancer Treatment
FDA Pre-Market Approval
FDA Class 3
·BSD 1000 HYPERTHERMIA SYSTEM
System, Rf/Microwave Hyperthermia, Cancer Treatment
FDA Pre-Market Approval
FDA Class 3
·BSD 1000 HYPERTHERMIA SYSTEM