Supply Of Electronic Items -Digital Storage Oscilloscope 70Mhz, 2 Channel, 12Bit, Digital Storage Oscilloscope 2 Channel Oscilloscope With 100 Mhz Bandwidth, Digital Storage Oscilloscope 100Mhz, 4 Channel, Isolated Dc Power Supply With Three Isolated Independent Output Channels, Single Channel Power Supply - 50 V, 3 A, Max 150 W, Two Channel Function, Arbitrary Waveform Generator With 10 Mhz Bandwidth, Two Channel Function, Arbitrary Waveform Generator With 25 Mhz Bandwidth, Digital Vernier Calliper, Digital Display, 150Mm, Digital Screw Gauge Or Micrometer, Digital Display, 0- 25Mm, Digital Stop Watch, Ammeter 10A, Voltmeter 500V, Digital Multimeter 1000V Ac Dc, Display 4-Digits Lcd, Digital Multimeter 6000 Counts Backlit Lcd, T-Rms, Benchtop Multimeter 5.5 Digit High Precision With Datalogging Trms 7 Inch Colour Touch Screen, Digital Clampmeter 1000A Ac Dc Trms, Tool Kit Set Including Drill Machine With Bits, Cutter, Hammer, Plier, Etc, Screw Driver Kit, Fume Extractor For Soldering Station, Soldering Station, Esd Safe, 70W, 200-480 Degree C, Battery Tester, Resistance Measurement, Regulated Power Supply, 30V, 5A, 3D Printer For Electrical And Physics Lab
Supply of Digital Ultrasonic Testing Equipment For Welded Rail Joints With Coloured Lcd Tft Screen, Trigonomet Rical Function And A-Scan Storage Along With Data Setup As Per Rdso Specification No. Rdso/M&C/Ndt/129/20 05 Rev-Ii, August 2014 With At & Fb Weld Test Piece For Smooth Usfd Testing Of Railway Track. Warranty Peri Od: 36 Months After The Date Of Delivery
Supply of Electronic Type Wheel Distance/ Wheel Back-To-Back Distance Measuring Gauge Similar To Model Wg-11 E With Tablet, Having An All-Metallic Construction. The Gauge Measures Wheel Distance Of Rolling Stock Wheel Sets With 0.1 Mm Resolution. The Unique Design Ensures Measurement Parallel To Wheel Axle And Square To Wheel Back Face. Specifications: Measuring Range : +-15 Mm From Standard. 0 Zero Set At Standard Setti Ng : 1600 Mm. Measuring Tips Left & Right : Made Of Carbide. Accuracy : +- 0.1 Mm. Least Count : 0.1 Mm. W Eight : 2 Kg. Approx. For B.G. Construction : All Metal Construction. Power Supply : Li Ion Rechargeable Battery. Display : Graphical Oled. Memory : 100 Readings. Operating Temperature : -10C To 60C. Data Storage : Wirele Ss Tablet For Data Storage. Battery Charging Provision : Type 5V Charging Port. Type C Usb With Battery Charge R Provided With Device. Tablet : Samsung Or Similar, Height Of Character : 11 Mm. Make/Brand: Pie/Esa/Bpi. Warranty Period: 30 Months After The Date Of Delivery
Supply of Digital Ultrasonic Testing Equipment Dwt For Welded Rail Joint With Lcd, Lcd Screen, Trigono Metric Functions And A- Scan Storage Along With Data Setup As Per Rdso Specification No M&C/Ndt/ 129/2005, Rev-Ii August 2014 With Standard Accessories Attached To Indent Uploaded Warranty Period: 30 Months Aft Er The Date Of Delivery
Annual Maintenance Service -Data Center Assets - Server With Enterprise Storage; Server With Enterprise Stoarge; As Oem Oem Authorised Service Provider Neither Oem Nor Asp
Supply of Cife Nucleic Acid Sequencing And Genotyping Service - Dna Sequencing; Animal; Nucleic Acids Dna Or Rna; To Be Collected By The Service Provider From The Buyer; Abi; 90% And Above; 2X; Undefined Low Throughput; Raw Data; Cloud Storage; 15 Days; System O..
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 Srph154052-Single Chamber Rate Responsive Pacemaker System Should Be Mri Conditional With Appropriate Bipolar Mri Conditional Lead. Should Have The Lat Est Technological Features To Provide Proportionate, Smooth And Appropriate Re Sponse Of Pacing Rate To Increased Metabolic Demand. Should Be Suitable For Use In Adult And Children. Should Have Sufficient Programming Flexibility For Using In Atri Um Where Sensitivity Should Be Adjustable To 0.25Mv Or Lower And / Or Ventricle An D Should Be Supplied With Low Profile Atrial / Ventricular Mri Compatible Lead. To B E Specified When Taking Delivery. The Lead Should Be Low Profile 7F Or Smaller Intr Oducer And Should Be Steroid Eluting. Should Be Capable Of High Energy Output Pa Cing With Pulse Amplitude Of Up To At Least 6.0V And Pulse Width Up To Atleast 1.0Ms. T He Pacing System Should Have Maximum Flexibility Of Programming, Data Storage An D Display For Ease Of Clinical Follow Up And Diagnosis Of Malfunction. Should Be Co Vered By Life Warranty. Providing Pacing Therapy For The Duration Of Patients Life Time. Should Provide Free Of Charge The Latest Programmer With Appropriate Soft Ware Which Should Have Facilities For Simultaneous Display Of Multiple Surface Ec G Leads, Intracardiac Electrograms, Event Markers, Electronic Calipers And For R Ecording The Same Both On Paper And In Electronic Storage Media E.G. Compact Disc S Etc., The Safety And Efficacy Of The Pacing System Should Be Documented In Scient Ific Publications. Unit:No
supply , installation , testing and commissioning Of Auto-Titrator For Nitrating Mixture Acid Analysis With Data Storage & Retrieval System Q3
Supply of Digital Ultrasonic Single Rail Tester With 09 Proves Coloured Single And Real A.Scan Use Each With Continuous Recording Of B.Scan Storage Of Each Probe A Long With Data Setups Model Multi Scan Sr-09 Warranty Period: 30 Months After The Date Of Deli Very
Supply of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Df - 4 Connector And Option Of Dual Shocking Coil.. Sr Ph 154066-Mri Conditional Dual Chamber Implantable Cardioverter Defibri Llator System With Appropriate Atrial And Ventricular Pace / Sense Leads With Df - 4 C Onnector And Option Of Dual Shocking Coil Leads And Accessories. System Should Hav E Advanced Features For The Reliable Detection And Management Of Ventricular Tach Ycardia And Ventricular Fibrillation, Including Features To Differentiate Supra-Ventr Icular Tachycardia From Ventricular Tachycardia And Features To Avoid Inappropriat E Shocks, Tiered Therapy Delivery, Choice Of Atp Protocols And Shock Energies, And S Hould Be Capable Of Delivering Maximum Energy Of 35J Or More And Should Have Featu Res For Management Of High Defibrillation Energy Requirement. Charge Times Should Be Within Clinically Acceptable Limits Throughout The Lifetime Of The Device.Leads Sho Uld Be Low Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Avail Able. Should Have Features For Automatically Alerting The Patient In The Event Of A Ba Ttery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Include Episode Details, Therapy Delivered And Results And Electrogram Storage And Should Be Comprehensive. Bradycardia Pacing Includi Ng Independently Programmable Parameters For High Output For Post-Shock Pacing Should Be Available. Warranty Terms Should Be Specified Clearly Along With The Quot Ation. Firms Should Submit Detailed Literature Of The Item In A Bulletin/Tutorial Forma T Which Should Contain All The Details About The Product. Compliance Statement Of E Ach Specification To Be Submitted. The Firm Quoting The Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacturer. The Manuf Acturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Th E Safety And Efficacy Of The Icd Device And The Lead In Clinical Use Should Be Documen Ted In Scientific Publications. All The Above Mentioned Specifications Are Essential An D Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:No
Supply of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System. Srph154064-Mri Conditional Dual Chamber Implantable Cardioverter Defibril Lator System With Appropriate Atrial And Ventricular Pace / Sense Leads And Option O F Dual Shocking Coil Leads And Accessories. System Should Have Advanced Features F Or The Reliable Detection And Management Of Ventricular Tachycardia And Ventricul Ar Fibrillation, Including Features To Differentiate Supra-Ventricular Tachycardia Fr Om Ventricular Tachycardia And Features To Avoid Inappropriate Shocks, Tiered Ther Apy Delivery, Choice Of Atp Protocols And Shock Energies, And Should Be Capable Of D Elivering Maximum Energy Of 35J Or More And Should Have Features For Management O F High Defibrillation Energy Requirement. Charge Times Should Be Within Clinically Ac Ceptable Limits Throughout The Lifetime Of The Device. Leads Should Be Low Profile An D Choice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Fea Tures For Automatically Alerting The Patient In The Event Of A Battery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Stora Ge Should Include Episode Details, Therapy Delivered And Results And Electrogram St Orage And Should Be Comprehensive. Bradycardia Pacing Including Independently Pr Ogrammable Parameters For High Output For Post-Shock Pacing Should Be Available. Warranty Terms Should Be Specified Clearly Along With The Quotation. Firms Should S Ubmit Detailed Literature Of The Item In A Bulletin/Tutorial Format Which Should Conta In All The Details About The Product. Compliance Statement Of Each Specification To B E Submitted. The Firm Quoting The Tender Should Submit A Letter Of Authorisation Fro M The Principal Firm/Original Equipment Manufacturer. The Manufacturer / Supplier Sh Ould Submit Proof Of Supply To A Major Government Institute. The Safety And Efficac Y Of The Icd Device And The Lead In Clinical Use Should Be Documented In Scientific Publ Ications. All The Above Mentioned Specifications Are Essential And Mandatory And Sho Uld Be Submitted At The Time Of Initial Tender Submission. Unit: No
Supply of 1 Data Logger Unit Storage Q3
Supply of Dicom Data Storage System Q3
Custom Bid For Services - Camc Of Digital Data Storage Boxes Along With Accessories Installed At Nia Hqrs New Delhi And Nia Branch Office Hyderabad For A Period Of 03 Years
Data Recovery And Data Wiping Service - Data Wiping; Tape Drive; Physical Physically Damaged Storage Media
Design, Development/Customization And Implementation Of A Software Solution For Document Management, Digitization/Scanning Of Documents, Storage, Retrieval Of Documents And Entry Of R And R Data Into Software Wrt Rehabilitation And Resettlement Of Af
