403 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Pre Market Approval
×
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid® Annular Closure Device - Model Number BAR-A8-8MM (2730815-A&), Barricaid® Annular Closure Device - Model Numb
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·BARRICAID ANULAR CLOSURE DEVICE (ACD)
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Annular Closure Device
Reherniation Reduction Device
FDA Pre-Market Approval
FDA Class 3
·Barricaid Anular Closure Device
Test, Fluorescence In Situ Hybridization (Fish), For Bladder Cancer Detection And Monitoring For Recurrence
FDA Pre-Market Approval
FDA Class 3
·UROVYSION BLADDER CANCER KIT
System, Test, Her-2/Neu, Nucleic Acid Or Serum
FDA Pre-Market Approval
FDA Class 3
·VYSIS PATH VYSION HER-2 DNA PROBE KIT
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·ONYX LIQUID EMBOLIC SYSTEM
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·HYDRON(R) (POLYMACON) HYDROPHILIC CONTACT LENSES
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·\YDRON(R) (POLYMACON) HYDROPHILIC CONTACT LENSES
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·ONYX LIQUID EMBOLIC SYSTEM (LES)
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·ONYX LIQUID EMBOLIC SYSTEM
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·Resolute Onyx Zotarolimus-Eluting Coronary Stent System
Embolization Agent, Vascular
FDA Pre-Market Approval
FDA Class 3
·Lava Liquid Embolic System (Lava LES)
Embolization Agent, Vascular
FDA Pre-Market Approval
FDA Class 3
·Lava Liquid Embolic System (Lava LES)
Embolization Agent, Vascular
FDA Pre-Market Approval
FDA Class 3
·Lava Liquid Embolic System (Lava LES)