4,487 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·LATITUDE NXT PATIENT MANAGEMENT SYSTEM
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·PSW 2202.U and NEO 2202.U
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·LATITUDE CONSULT SYSTEM
Intrasaccular Flow Disruption Device
FDA Pre-Market Approval
FDA Class 3
·Woven EndoBridge (WEB) Aneurysm Embolization System
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·CARELINK HOME MONITOR MODEL 2490C, CARDIOSIGHT READER MODEL 2020A, CAELINK NETWORK DEVICE
Intrasaccular Flow Disruption Device
FDA Pre-Market Approval
FDA Class 3
·Woven EndoBridge (WEB) Aneurysm Embolization System
Intrasaccular Flow Disruption Device
FDA Pre-Market Approval
FDA Class 3
·Woven EndoBridge (WEB) Aneurysm Embolization System
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·Renamic Neo Programmer
Intrasaccular Flow Disruption Device
FDA Pre-Market Approval
FDA Class 3
·(WEB) Aneurysm Embolization System
Intrasaccular Flow Disruption Device
FDA Pre-Market Approval
FDA Class 3
·Woven EndoBridge (WEB) Aneurysm Embolization System
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC CARELINK MONITOR, MYCARELINK PATIENT MONITOR
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·REVEAL DX, REVEAL XT
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC MODELS 2490C CARELINK REMOTE HOME MONITORS
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·MYCARELINK SMART MONITOR AND THE MYCARELINK HEART APPLICATION
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·LATITUDE PATIENT MANAGEMENT SYSTEM, WAVE COMMUNICATOR MODEL 6290; NXT SYSTEM SEVER SOFTWARE MODEL 6460
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·PSW 2201.U/1 and NEO 2201.U/1
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·LATITUDE CONSULT SYSTEM
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·LATITUDE INDUCTIVE COMMUNICATOR ; LATITUDE PROGRAMMER/RECORDER/MONITOR (PRM)
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·PARADYM RF VR 9250 PARADYM RF DR 9550
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·MODEL 3140 ZOOM WIRELESS TRANSMITTER AND MODEL 3120 ZOOM LATITUDE PROGRAMMER/RECORDER/MONITOR (PRM)