Platinium™ – the world's longest projected longevity.1–4
Platinium™ is an ICD with proven therapeutic functions.
Featuring
Parad+™
Protecting patients for over 20 years.
Featuring
BTO™
Unlocks Brady and Tachy therapies in the slow VT zone.
Featuring
SafeR™
Avoids deleterious effects of excessing RV pacing.5
World's longest projected longevity1–4
Platinium™ VR
- Longevity = 14.3 years
Platinium™ DR
- Longevity = 13.1 years
Longevity calculations are based on real life pacing conditions.6
Visit the Cardiac Device Longevity website for more information.
Backed by warranty7
Platinium™ VR
- Warranty = 11 years
Platinium™ DR
- Warranty = 9 years
Warranty applies regardless of pacing conditions and therapy frequency.7
Breakthrough technology that stands the test of time
- 40% reduced electronic consumption8
- 20% improved battery capacity8
- Reforming-free capacitors mean zero energy is wasted
Small size
Platinium™ is designed to facilitate the implant experience and improve patient comfort.
- Rounded edges
- Reduced pocket size
- Allows for smaller incision
- Better fit for replacements
Ergoform™ design
Platinium™ with its smooth and curved header is designed for natural lead wrap around.
Built on proven technology
Platinium™ family is built on the heritage of MicroPort CRM technology: the PARADYM™ platform. The PARADYM™ pacemaker platform has been proven in practice.9
99.96% cumulative survival 6 years after implantation.9
Parad+™
Protecting patients for over 20 years.
- World’s first dual-chamber discrimination algorithm
- Best in class 99% specificity10
- Low inappropriate shock rate5
- Immediate protection with Parad+™ out-of-the-box setting
SafeR™
Avoids deleterious effects of excessing RV pacing.5
- Manages all types of AV Block
- Activated automatically on implant
- More than 96% preserved intrinsic conduction5
BTO™
Unlock Brady and Tachy therapies in the slow VT zone
- 96% specificity in slow VT zone11
- A proof of Parad+™ discrimination performance
Caution: Federal law (USA) restricts this device to sale by or on the order of a physician. For indications, contraindications, precautions and warnings for each devices, please refer to the product manual.
Related products:
Orchestra Plus Programmer™; Smartview Remote Monitoring System™; Vega™; Xfine™
References
- Medtronic – VISIA AF MRI™ VR SureScan™ DVFB1D4 Device manual M961177A001 B 2015-07-02. EVERA™ XT DR DDBB1D4 Device manual M946302A001 F 2014-03-11.
- (EU): Biotronik – ILIVIA™ 7 VR-T, VR-T DX, DR-T, HF-T, HF-T QP (ProMRI®) Technical Manual 417641 Revision: D (2016-08-09).
(US): Biotronik – ILIVIA ProMRI™ Family of ICDs and CRT-Ds – Technical Manual M4206-B 01/18 / MN070 1/23/18. - (EU): Saint Jude Medical – Bradycardia and Tachycardia Devices – Help Manual – June 2013 Art 60033180/A.
(US): Saint Jude Medical – Bradycardia and Tachycardia Devices – Help Manual – November 2017 ARTEN100161329 A. - (EU): Boston Scientific – Physician’s technical manual RESONATE™ HF ICD, RESONATE™ EL ICD, PERCIVA™ HF ICD, PERCIVA™ EL ICD, CHARISMA™ EL ICD, VIGILANT™ EL ICD, MOMENTUM™ EL ICD – Implantable Cardiovertor Defibrillator – 360204-001 EN Europe 2016-09.
(US): Boston Scientific – Physician’s technical manual AUTOGEN™ EL ICD, DYNAGEN™ EL ICD, DYNAGEN™ MINI ICD, INOGEN™ EL ICD, INOGEN™ MINI ICD, ORIGEN™ EL ICD, ORIGEN™ MINI ICD, INCEPTA™ ICD, ENERGEN™ ICD, PUNCTUA™ ICD, TELIGEN™ 100 ICD – Implantable Cardiovertor Defibrillator – 359403-004 EN US 2017-04. - Kolb C, et al. Reduced Risk for Inappropriate Implantable Cardioverter-Defibrillator Shocks With Dual-Chamber Therapy Compared With Single-Chamber Therapy. Results of the randomized Option study. JACC Heart Failure 2014;2:611–19.
- Functioning conditions for projected longevity (conditions based on MicroPort CRM data on file): DR models: Pacing in SafeR mode, 30% in atrium, 6% in ventricle, at 60 min-1, 600Ω, 2.5V, 0.35ms, 4 max shocks per year, sensor OFF. VR models: Pacing in VVI mode 6% at 40 min-1, 600Ω, 2.5V, 0.35ms, 4 max shocks per year, sensor OFF. Longevities are calculated by taking into account 6 months storage with the following conditions: Remote ON: daily check, 4 follow-ups and 5 full alert reports per year. RF telemetry ON: 45min + 15min at discharge + 15min in-clinic quarterly FU.
- For more details please refer to the following document supplied with the device: EU U666 – LIMITED WARRANTY for PLATINIUM ICD & CRT-D devices; US U668 – LIMITED WARRANTY for PLATINIUM ICD & CRT-D devices.
- Versus previous ICD generation (Paradym RF™).
- MicroPort CRM Product Performance Report.
- Hintringer F, et al. Comparison of the Specificity of Implantable Dual Chamber Defibrillator Detection Algorithms. Pacing Clin Electrophysiol. 2004;27:976–82.
- Sadoul N, et al. Incidence and clinical relevance of slow ventricular tachycardia in implantable cardioverter-defibrillator recipients: an international multicenter prospective study. Circulation. 2005;112:946–53.