Supply Of 25W Vhf Digital Radio Set As Per Rdso Specification No. Rdso/Spn/Tc107-2018 Ver 2.1 Or Latest. As Per Rdso Specification Clause 10.0 The Following Are Required, 10.1 Frequency Range 146 - 174 Mhz, 10.2- As Per Clause 5D, 10.6 - Programming Kit With Software And 10.7 - English Language Required For Cha Nnel No Announcement/Display, Excluding Antenna, Rf Cable, Battery Only Radio May Be Supplied.Make: Kenwo Od, Motorola, Hyt, Alinico Or Similar. Warranty Period Upto 30 Months From The Date Of Supply. Inspection By Tpi. The Oem Authorisation Certificate Shall Be Submitted Along With The Quote In The Tender For Technical Scrutiny. W Arranty Period: 30 Months After The Date Of Delivery
Supply of 25Watt Vhf Digital Radio Set With Suitable Smps Power Supply Unit, Antenna And Antenna Cable As Per Rdso/Spn/Tc/107/2018 Ver 2 Or Later, 1 Frequency Range 146 To 174 Mhz, 2 Technical Parameter As Per Clause 5 D Of Aforesaid Rdso Specification. 3Cable Length To Be Supplied 30 Mtr, Rg 217 Low Loss Cable. 4 S Mps Float & Boost Charging Mode Shall Be Of Min. 15 A Output And Suitable For Charging 12 V/120 Ah Capacity Battery Along With Programming Kit-2 Nos With Software One No., Spot Frequency 147.975 Mhz. Firm Must Submit Compliance Sheet As Per Rdso Specification As Well As Documents Related To As Per 5.7.4.1 Of Rdso Specs, Di Gital Protocol Shall Be Etsi Dmr Open Standard, And Oem Should Be Category-1 Manufacturer Status Membe R Of Dmr Association & As Per 5.7.4.2 Of Rdso Specs, Set Shall Have Iop Certification Issued By Dmr Associati On . Warranty Period: 30 Months After The Date Of Delivery
Supply of Srph154036-Mri Conditional Dual Chamber Pacemaker Rate Responsive Ddd R With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead Mri Conditi Onal With Life Warranty Provision Of Pacing Therapy For The Use Of The Patients Lif E-Time Including Any No. Of Pulse Generator Replacements As Clinically Required. S Hould Have The Latest Technological Features To Provide Proportionate, Smooth A Nd Appropriate Response Of Pacing Rate To Increased Metabolic Demand, Should Pr Ovide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Mode S Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibilit Y Of Programming Including Minimal Av Delay Of 30Msec Or Less And Atrial Sensitivit Y Of 0.2Mv Or Less, Detailed Data Storage With Easy Retrieval And Display Of Advanc Ed Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capabl E Of Programming For Prolonging Longevity And Maximal Cost Effectiveness. Shoul D Be Capable Of Providing Reliable Ventricular Capture With Lowest Battery Drain S O As To Provide Maximum Longevity Of The Pacing System. Preferably As An Automati C Feature Where The Pulse Generator Can Perform A Periodic Threshold Test And R Eliably Verify Ventricular Capture And Adjust Ventricular Pulse Output Parameter S To Minimize Battery Drain Without Compromising Patient Safety. Should Have Feat Ures For Automatic Management Of Arrhythmias Including Pacemaker Mediated Arr Hythmias As Well As Automatic Mode Switching Mode Switch Should Be To And From Ddd To Ddi/Vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automat Ic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias. Sho Uld Have Algorithms To Promote Intrinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.E. Up To At Least 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Repro Gramming Should Be Rendered As Effective As Possible Through Provision Of Adequ Ate Information Management Systems On The Programmer. Mri Compatible Leads Sho Uld Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type 7F Or Smaller Introducer Individually. Leads Should Be From The Same Manufacture R I.E. Manufactured By The Same Company As The Pulse Generator, Not Outsourced A Nd Marketed By Another Company. Pulse Generator And Leads Should Be Suitable Fo R Adult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof O F Supply To A Major Government Institute. Publications Supporting The Safety And E Fficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Available In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanently In The Hospital. The Programmer Should Have Fac Ilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intracardiac Electr Ograms, Event Markers, Electronic Calipers And For Recording The Same Both On P Aper And In Electronic Storage Media E.G. Compact Disc Etc., Unit:No
Supply Of Compactlogix 5380 Controller Product Code: 5069-L306er Q3, Power Terminal Rtb Kit Product Code: 5069-Rtb64- Screw Q3, End Capproduct Code: 5069-Ecr Q3, Flex Ethernet/Ip Adapterproduct Code: 1794-Aentr Q3, Ethernet/Ip Tap W/3 Copper Ports Product Code: 1783-Etap Q3, Flex Terminal Base For Rtd Moduleproduct Code: 1794-Tb3g Q3, Flex Terminal Base Product Code: 1794- Tb32 Q3, Flex 16 Ch- Di Moduleproduct Code: 1794- Ib16 Q3, Flex 16 Ch-Do Module Product Code: 1794- Ob16 Q3, Flex 8-Ch Rtd Moduleproduct Code: 1794- Irt8 Q3, Studio 5000 Programming Software Product Code: 9324M-Rldt10m Q3, Serial Communication Cable Product Code: 1763-Nc01 Q3, Micrologix 1400 Ac Powered Product Code: 1766-L32bwa Q3, Micrologix 1400 Dc Powered Product Code: 1766-L32bxb Q3