2,568 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·EXOSEAL VASCULAR CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL ELITE VHD/ES DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·ANGIO-SEAL(TM)[1] HEMOSTATIC PUNCTURE CLOSURE DEVICE
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·StarClose SE Vascular Surgical System
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·cobas HPV Test
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·EXOSEAL VASCULAR CLOSURE DEVICE (VCD)
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
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR ASSAY
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·PROLIEVE THERMODILATATION SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·CELT ACD PLUS Vascular Closure Device
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·Angio-Seal Vascular Closure Devices
System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy
FDA Pre-Market Approval
FDA Class 3
·UROLOGIX TARGIS SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·Cardiva VASCADE Family
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·EXOSEAL VASCULAR CLOSURE DEVICE
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·VIRAPAP HUMAN PAPILLOMAVIRUS DNA DETECTION KIT
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASCADE VASCULAR CLOSURE SYSTEM
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DUETT PRO SEALING DEVICE (MODEL 1010) AND DIAGNOSTIC DUETT PRO SEALING DEVICE (MODEL 2210)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·EXOSEAL vascular Closure Device
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·7F FISH-SP DEVICE