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Modular Bipolar prosthesis sterilized size 37-55 mm with Calcar stem, bone Cement 40 mg, cement restrictor and Centralizer with disposables sterile Cement gun / Syringe Kit and Pulse lavage with all relevant Instrumentation Set

Pulse Lavage Built in battery with on/off button, both short fan spray tip ( cone tip ) with splash shield & long coaxial canal tip connectors should be inside pack ( PVC Medical grade) , both irrigation and suction tubes ( 3 Mtr ) should have clamps to prevent the leakage of fluid , Speed adustable high ( 110 - 1400 ml/min cone tip & 1000 - 1300 ml/mm coaxial tip ) to low flow rate 700 ml/mm, Pressure should be 15 psi, Pulse rate 1500-1700 cycle/min, EU CE certify with 4 digit notified body.

Pulse oxymeter , Pulse SPO2

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攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀됀✀딀⬀Ȁ✁̀⬁㜀✁㠀⬁褀✁言⬁謀⼁관✁글⬁팀✁퐀⬁ᰀ✂ᴀ⬂帀✂开⬂輀✂退⬂ༀᨃက⬃爀✃猀⬃씀✃였⬃☀ऄDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have Quadripolar lead for LV pacing  Must have all basic programmable parameters with following special features  Facility of ATP during charging for defibrillation  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay  Must have fluid monitoring system  The leads should be steroid eluting  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+É'Ê+ė'Ę+Ō'ō+ƞ'Ɵ+Ơ/ǂ'ǃ+Ǩ'ǩ+ȱ'Ȳ+ɳ'ɴ+ʤ'ʥ+̤̥+·'Έ+Ϛ'ϛ+Ιᜉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 猀攀瀀愀爀愀琀攀 瀀爀漀最爀愀洀洀愀戀氀攀 刀嘀Ⰰ 䰀嘀 氀攀愀搀 愀洀瀀氀椀琀甀搀攀Ⰰ 瀀甀氀猀攀 眀椀搀琀栀 愀渀搀 嘀嘀 搀攀氀愀礀਀뜀⃰吀栀攀 猀椀稀攀 漀昀 愀琀爀椀愀氀 Ⰰ 刀嘀 氀攀愀搀 洀甀猀琀 戀攀 㤀䘀 漀爀 氀攀猀猀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀✀⬀ഀ✁฀⬁嬀✁尀⬁ꐀ✁ꔀ⬁✁⬁ᜀ✂᠀⬂需ᨂ頀⬂切✂ff⬂䴀✃一⬃글ःDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay  The size of atrial , RV lead must be 9F or less  The leads should be steroid eluting and should be both bipolar and unipolar  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+ð'ñ+Ģ'ģ+Ű'ű+ƹ'ƺ+ǻ'Ǽ+Ȭ'ȭ+ʬʭ+̏'̐+͢'ͣ+Сᤉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 猀攀瀀愀爀愀琀攀 瀀爀漀最爀愀洀洀愀戀氀攀 刀嘀Ⰰ 䰀嘀 氀攀愀搀 愀洀瀀氀椀琀甀搀攀Ⰰ 瀀甀氀猀攀 眀椀搀琀栀 愀渀搀 嘀嘀 搀攀氀愀礀 愀渀搀 猀栀漀甀氀搀 栀愀瘀攀 昀漀氀氀漀眀椀渀最 猀瀀攀挀椀愀氀 昀攀愀琀甀爀攀਀뜀⃰䴀甀猀琀 栀愀瘀攀 愀氀最漀爀椀琀栀洀 昀漀爀 䄀䘀 猀甀瀀瀀爀攀猀猀椀漀渀 眀椀琀栀 瀀爀漀最爀愀洀洀愀戀氀攀 愀甀琀漀洀愀琀椀挀 洀漀搀攀 猀眀椀琀挀栀 戀愀猀愀氀 爀愀琀攀਀뜀⃰吀栀攀 猀椀稀攀 漀昀 愀琀爀椀愀氀 愀渀搀 刀嘀 氀攀愀搀 洀甀猀琀 戀攀 㜀䘀 漀爀 氀攀猀猀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀Ԁ✁؀⬁愀✁戀⬁销✁阀⬁✁⬁Ⰰ✂ⴀ⬂渀✂漀⬂鼀✂ꀀ⬂ἀᨃ ⬃舀✃茀⬃픀✃혀⬃㘀ऄDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special feature  Must have algorithm for AF suppression with programmable automatic mode switch basal rate  The size of atrial and RV lead must be 7F or less  The leads should be steroid eluting and should be both bipolar and unipolar  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+Ě'ě+Ŷ'ŷ+ƪ'ƫ+Ǹ'ǹ+Ɂ'ɂ+ʃ'ʄ+ʴ'ʵ+̴̵+Η'Θ+Ϫ'ϫ+жᤉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 猀攀瀀愀爀愀琀攀 瀀爀漀最爀愀洀洀愀戀氀攀 刀嘀Ⰰ 䰀嘀 氀攀愀搀 愀洀瀀氀椀琀甀搀攀Ⰰ 瀀甀氀猀攀 眀椀搀琀栀 愀渀搀 嘀嘀 搀攀氀愀礀 愀渀搀 猀栀漀甀氀搀 栀愀瘀攀 昀漀氀氀漀眀椀渀最 猀瀀攀挀椀愀氀 昀攀愀琀甀爀攀਀뜀⃰䴀甀猀琀 栀愀瘀攀 昀愀挀椀氀椀琀礀 昀漀爀 愀甀琀漀洀愀琀椀挀 䰀嘀 漀渀氀礀 愀渀搀 䈀䤀嘀 瀀愀挀椀渀最 ☀ 愀甀琀漀洀愀琀椀挀 䄀嘀Ⰰ 嘀嘀 搀攀氀愀礀਀뜀⃰吀栀攀 猀椀稀攀 漀昀 愀琀爀椀愀氀 愀渀搀 刀嘀 氀攀愀搀 洀甀猀琀 戀攀 䐀䘀ⴀ㐀 挀漀洀瀀愀琀椀戀氀攀 愀渀搀 䰀嘀 氀攀愀搀 焀甀愀爀搀椀瀀漀氀愀爀⸀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀Ԁ✁؀⬁堀✁夀⬁ꨀ✁꬀⬁✁豈⬁䄀✂䈀⬂茀✂萀⬂됀✂딀⬂㐀ᨃ㔀⬃需✃頀⬃✃⬃䬀ऄDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special feature  Must have facility for automatic LV only and BIV pacing & automatic AV, VV delay  The size of atrial and RV lead must be DF-4 compatible and LV lead quardipolar.  The leads should be steroid eluting and should be both bipolar and unipolar  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+Ě'ě+ŭ'Ů+ƿ'ǀ+ȍ'Ȏ+ɖ'ɗ+ʘ'ʙ+ˉ'ˊ+͉͊+ά'έ+Ͽ'Ѐ+δᜉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 猀攀瀀愀爀愀琀攀 瀀爀漀最爀愀洀洀愀戀氀攀 刀嘀Ⰰ 䰀嘀 氀攀愀搀 愀洀瀀氀椀琀甀搀攀Ⰰ 瀀甀氀猀攀 眀椀搀琀栀 愀渀搀 嘀嘀 搀攀氀愀礀 愀渀搀 猀栀漀甀氀搀 栀愀瘀攀 昀漀氀氀漀眀椀渀最 猀瀀攀挀椀愀氀 昀攀愀琀甀爀攀਀뜀⃰吀栀攀 䰀嘀 氀攀愀搀 洀甀猀琀 戀攀 儀甀愀搀爀椀瀀漀氀愀爀⸀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀Ԁ✁؀⬁⠀✁⤀⬁瘀✁眀⬁뼀✁쀀⬁Ā✂Ȁ⬂㈀✂㌀⬂눀ᨂ대⬂ᔀ✃ᘀ⬃栀✃椀⬃준ःDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special feature  The LV lead must be Quadripolar.  The leads should be steroid eluting and should be both bipolar and unipolar  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+Ě'ě+Ľ'ľ+Ƌ'ƌ+ǔ'Ǖ+Ȗ'ȗ+ɇ'Ɉ+ˇˈ+̪'̫+ͽ';+;ᜉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 䄀甀琀漀洀愀琀椀挀 䰀嘀 漀渀氀礀 愀渀搀 䈀䤀嘀 瀀愀挀椀渀最 ☀ 䄀甀琀漀洀愀琀椀挀 䄀嘀Ⰰ 嘀嘀 搀攀氀愀礀਀뜀⃰吀栀攀 䰀嘀 氀攀愀搀 洀甀猀琀 戀攀 儀甀愀搀爀椀瀀漀氀愀爀⸀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀케✀퀀⬀✀⬀䀀✁䄀⬁褀✁言⬁쬀✁찀⬁ﰀ✁ﴀ⬁簀ᨂ紀⬂✂⬂㈀✃㌀⬃錀ःDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have Automatic LV only and BIV pacing & Automatic AV, VV delay  The LV lead must be Quadripolar.  The leads should be steroid eluting and should be both bipolar and unipolar  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+ä'å+ć'Ĉ+ŕ'Ŗ+ƞ'Ɵ+Ǡ'ǡ+ȑ'Ȓ+ʑʒ+˴'˵+͇'͈+Σᤉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 䄀甀琀漀洀愀琀椀挀 䰀嘀 漀渀氀礀 愀渀搀 䈀䤀嘀 瀀愀挀椀渀最 ☀ 䄀甀琀漀洀愀琀椀挀 䄀嘀Ⰰ 嘀嘀 搀攀氀愀礀਀뜀⃰䴀甀猀琀 䠀愀瘀攀 昀氀甀椀搀 䴀漀渀椀琀漀爀椀渀最 昀攀愀琀甀爀攀਀뜀⃰吀栀攀 䰀嘀 氀攀愀搀 洀甀猀琀 戀攀 儀甀愀搀爀椀瀀漀氀愀爀⸀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀케✀퀀⬀✀⬀ᜀ✁᠀⬁攀✁昀⬁글✁꼀⬁✁⬁℀✂∀⬂ꄀᨂꈀ⬂Ѐ✃Ԁ⬃圀✃堀⬃렀ःDCGI APPROVED WITH US FDA/ C.E APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION  Must have Automatic LV only and BIV pacing & Automatic AV, VV delay  Must Have fluid Monitoring feature  The LV lead must be Quadripolar.  The leads should be steroid eluting and should be both bipolar and unipolar  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available/n#o/ž'Ÿ+ä'å+ĉ'Ċ+Ĭ'ĭ+ź'Ż+ǃ'DŽ+ȅ'Ȇ+ȶ'ȷ+ʶʷ+̙'̚+ͬ'ͭ+Σᬉ唀匀 䘀䐀䄀⼀䌀䔀 䄀倀倀刀伀嘀䔀䐀 䈀䤀嘀䔀一吀刀䤀䌀唀䰀䄀刀 倀䄀䌀䔀䴀䄀䬀䔀刀 ⬀ 䤀䌀䐀 ⠀䌀伀䴀䈀伀 䐀䔀嘀䤀䌀䔀⤀ 圀䤀吀䠀 䄀吀刀䤀䄀䰀Ⰰ 刀嘀Ⰰ 䰀嘀 䰀䔀䄀䐀匀 䄀一䐀 䄀䰀䰀 䄀䌀䌀䔀匀匀伀刀䤀䔀匀 刀儀唀䤀刀䔀䐀 䐀唀刀䤀一䜀 䤀䴀倀䄀一吀䄀吀䤀伀一਀뜀⃰䴀甀猀琀 栀愀瘀攀 䄀甀琀漀洀愀琀椀挀 䰀嘀 漀渀氀礀 愀渀搀 䈀䤀嘀 瀀愀挀椀渀最 ☀ 䄀甀琀漀洀愀琀椀挀 䄀嘀Ⰰ 嘀嘀 搀攀氀愀礀਀뜀⃰䴀甀猀琀 䠀愀瘀攀 昀氀甀椀搀 䴀漀渀椀琀漀爀椀渀最 昀攀愀琀甀爀攀਀뜀⃰吀栀攀 䰀嘀 氀攀愀搀 洀甀猀琀 戀攀 儀甀愀搀爀椀瀀漀氀愀爀⸀਀뜀⃰吀栀攀 氀攀愀搀猀 猀栀漀甀氀搀 戀攀 猀琀攀爀漀椀搀 攀氀甀琀椀渀最 愀渀搀 猀栀漀甀氀搀 戀攀 戀漀琀栀 戀椀瀀漀氀愀爀 愀渀搀 甀渀椀瀀漀氀愀爀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 戀漀琀栀 愀挀琀椀瘀攀 愀渀搀 瀀愀猀猀椀瘀攀 昀椀砀愀琀椀漀渀 刀䄀 ☀ 刀嘀 攀渀搀漀挀愀爀搀椀愀氀 氀攀愀搀猀਀뜀⃰匀栀漀甀氀搀 栀愀瘀攀 攀瀀椀挀愀爀搀椀愀氀 氀攀愀搀 昀漀爀 攀瀀椀挀愀爀搀椀愀氀 䰀嘀 氀攀愀搀 椀洀瀀氀愀渀琀愀琀椀漀渀਀뜀⃰刀攀瀀氀愀挀攀洀攀渀琀 眀愀爀爀愀渀琀礀 渀漀琀 氀攀猀猀 琀栀愀渀 ㌀ ⬀ ㈀ 礀攀愀爀猀਀뜀⃰䐀椀爀攀挀琀 瀀爀攀猀攀渀挀攀 漀昀 倀愀爀攀渀琀 䌀漀洀瀀愀渀礀 椀渀 䤀渀搀椀愀 ⠀渀漀琀 漀渀氀礀 琀栀爀漀甀最栀 琀栀攀 搀椀猀琀爀椀戀甀琀漀爀猀 ⤀ 愀渀搀 挀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 椀琀猀 琀爀愀椀渀攀搀 琀攀挀栀渀椀挀愀氀 瀀攀爀猀漀渀 昀漀爀 攀愀挀栀 椀洀瀀氀愀渀琀愀琀椀漀渀 眀栀攀渀 攀瘀攀爀 爀攀焀甀椀爀攀搀 愀渀搀 昀漀爀 昀漀氀氀漀眀 甀瀀 瀀爀漀最爀愀洀洀椀渀最 眀栀攀渀 椀琀 椀猀 爀攀焀甀椀爀攀搀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 瀀爀漀瘀椀搀攀 愀琀 氀攀愀猀琀 漀渀攀 瀀爀漀最爀愀洀洀攀爀 攀砀挀氀甀猀椀瘀攀氀礀 琀漀 琀栀攀 挀愀爀搀椀漀氀漀最礀 搀攀瀀琀⸀਀뜀⃰䌀漀洀瀀愀渀礀 洀甀猀琀 焀甀漀琀攀 漀渀氀礀 琀栀攀 氀愀琀攀猀琀 洀漀搀攀氀 漀昀 搀攀瘀椀挀攀猀 挀漀洀洀攀爀挀椀愀氀氀礀 愀瘀愀椀氀愀戀氀攀⼀洀⌀渀⼀褀✀言⬀케✀퀀⬀✀⬀⼀ᔀ⬁ᜀ✁᠀⬁攀✁昀⬁글✁꼀⬁✁⬁℀✂∀⬂ꄀᨂꈀ⬂Ѐ✃Ԁ⬃圀✃堀⬃렀ः