318 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·MFC-CPRD Cable Assembly used with X Series and R Series Device
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Zoll R series OneStep CPR Cable, R Series Onestep Pacing Cable, R Series MFC (Multi-Function Cable), Multifunction Thera
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·Onyx Liquid Embolic System
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·ONYX LIQUID EMBOLIC SYSTEM
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SLS SPECTRANETICS LASER SHEATHS
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
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·CVX-300 EXCIMER LASER VERSION V3.7.12/V3.8.12
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SLS / GlideLight
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·Apollo Onyx Delivery Micro Catheter
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·Spectranetics Laser Sheath (SLS ll/GlideLight)
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATHS (SLS)
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·ONYX LIQUID EMBOLIC SYSTEM
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·Apollo Onyx Delivery Micro Catheter
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·Apollo Onyx Delivery Micro Catheter, 1.5cm, Straight/Apollo Onyx Delivery Micro Catheter, 3.0cm, Straight
Agent, Injectable, Embolic
FDA Pre-Market Approval
FDA Class 3
·Onyx Liquid Embolic System
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·Spectranetics Laser Sheath (SLS) II and GlideLight Laser Sheath
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATH II PRODUCTS
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATHS
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANTICS SLS II LASER SHEATH