531 results
·
45ms
·
Sources: EU EUDAMED, US FDA
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX ACE VASCULAR CLOSURE DEVICE (MYNX ACE)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNXGRIP VASCULAR CLOSURE DEVICES
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·THE CLOSER AK 6 FR. SMC DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNXGRIP VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·D-Stat Flowable hemostat
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·CLOSER VASCULAR SEALING SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASCULAR SOLUTIONS DUETT SEALING DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLATFORM AND ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS PLATFORM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·Perclose ProGlide Suture-Mediated Closure System
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MynxGrip Vascular Closure Device
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL ES DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PERCLOSE A-T MONOFILAMENT 6 FR. SUTURE MEDIATED CLOSURE (SMC) SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·PERCLOSE PROGLIDE SUTURE MEDIATED CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·MYNX VASCULAR CLOSURE DEVICE PRODUCT FAMILY
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DIAGNOSTIC DUETT SEALING DEVICE, MODEL 2200; DIAGNOSTIC DUETT PRO SEALING DEVICE, MODEL 2210; AND D-STAT FLOWABLE HEMOS0