51 results · 42ms · Sources: EU EUDAMED, US FDA

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