51 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Pre Market Approval
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Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CADENCE(R) TIERED THERAPY DEFIBRILLATOR SYSTEM
FDA Pre-Market Approval
MEDTRONIC MODEL 7273 GEM II DR DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM WITH MODEL 9964 (GEM II DR) AP
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·THINLINE(TM)II/FINELINE(TM) II LEADS
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·THINLINE II/ FINELINE II
FDA Pre-Market Approval
MEDTRONIC GEM II VR MODEL 7229 SINGLE CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK
FDA Pre-Market Approval
GEM II DR MODEL 7273
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT TM II, MICRO STENT TM II XL, GFX TM, GFX TM XL
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT TM II, MICRO STENT TM II XL, GFX TM, GFX TM XL
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Stratos LV CRT-P / Stratos LV-T CRT-P / Corox OTW BP Lead / Corox OTW-S BP Lead
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Dromos DR/DR-A and Dromos SR/SR-B Cardiac Pacing System
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Tupoa LV/ATX & Kronos LV-T / CRT-D & Corox OWT Steroid LV Pacing Lead
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Phylax Implantable Cardioverter Defibrillator System
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·METROSOFT(TM) II (POLYMACON) HYDROPHILIC CONTACT
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·METROSOFT(TM) II (POLYMACON) HYDROPHILIC CONTACT
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·METROSOFT(TM) II (POLYMACON) HYDROPHILIC CONTACT
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·METROSOFT(TM) II (POLYMACON) HYDROPHILIC CONTACT
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 282-04Y NOVA(TM)II
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·METROSOFT(TM) II (POLYMACON) HYDROPHILIC CONTACT
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·METROSOFT(TM) II (POLYMACON) HYDROPHILIC CONTACT