77 results · 21ms · Sources: EU EUDAMED, US FDA

DYNABITE CARDIOVASCULAR BIOPSY FORCEPS

FDA 510(k)
FDA Class 2 ·Cardiovascular

Biopsy Forceps

FDA 510(k)
FDA Class 2 ·Cardiovascular

CORDIS BIPAL BIOPSY FORCEPS

FDA 510(k)
FDA Class 2 ·Cardiovascular

MYOCARD BIOPSY FORCEP

FDA 510(k)
FDA Class 2 ·Cardiovascular

CORDIS BIOPSY FORCEPS

FDA 510(k)
FDA Class 2 ·Cardiovascular

CORDIS BIPAL 7 BIOPSY FORCEPS WITH A INLINE HANDLE

FDA 510(k)
FDA Class 2 ·Cardiovascular

AMPLATZER TorqVue 45x45 Delivery Sheath

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD Intraosseous Infusion System

FDA 510(k)
FDA Class 2 ·General Hospital

Sentimag System, Sentimark Magnetic Marker Systerm

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

FDA Pre-Market Approval
FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED LINER

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

FDA Pre-Market Approval
FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED ACETABULAR LINER

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

FDA Pre-Market Approval
FDA Class 2 ·OSTEONICS CONSTRAINED ACETABULAR INSERT

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

FDA Pre-Market Approval
FDA Class 2 ·S-ROM POLY-DAIL CONSTRAINED LINER

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

FDA Pre-Market Approval
FDA Class 2 ·S-ROM POLY-DIAL CONSTRAINED LINER

Device, Biopsy, Endomyocardial

FDA classification
FDA Class 2 ·Device, Biopsy, Endomyocardial

Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt

FDA classification
FDA Class 2 ·Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt

Scaffold, Partial Medial Meniscal Defects Extending Into The Red/White Zone, Resorbable Bovine Collagen

FDA classification
FDA Class 2 ·Scaffold, Partial Medial Meniscal Defects Extending Into The Red/White Zone, Resorbable Bovine Collagen