Design, Manufacture, Supply, Installation, Testing And Commissioning Of Pasenger Escalator For Ver Tical Hieght Of 6 Mtr Complete With All Associated Accessories And Safety Device Etc. As Per Rdso Specification No. Rdso/Pe/Spec/Tl/0095Rev-32019 Or Latest. Make- Schindler/ Kone/ Otis/ Johnson Or Similar Warranty Period: 30 Months After The Date Of Delivery
Supply of 640 Electrical Safety Devices And Accessories Insulating Mats For Electrical Purposes As Per Is 15652 Q3
Supply of 400 Dressing Wound Care 10Cm X10cm Box Of 5 Q3 Laparscope Mesh Fixation Device Absorbable Tacker 5Mm Shaft With 20-30 Takcs Q3 Laparoscope Absortable Mesh Fixation Device Non Absorbable Tacker 5Mm Shaft With 20- 30 Tacks Q3 Proximate Liner Cutter With Safety Lock Out 75Mm Q3 33Mm Heamorrhoidal Circular Stapler With 3.5 To 4.8Mm Staple Height Q3
Supply Of Personal Floatation Device Life Jacket Made Of Polyurethane Foam, Torch Or Emergency Light Solar Enabled, Safety Gloves Canvas/Leather 30 Mtrs 10/11 Mm Bob Nylon Rope, Lifebuoys, Oars & Rowlocks, Paddles, Anchors, Galvanized Metal Bucket Or Bailer, Outboard Motor Minimum 30 Hp, Dcp Fire Extinguisher, Emergency Spot Light With Minimum 12 Hours Run Time, Tool Kit Colt Cutier, Pliers, Screw Driver Set, Axe/Hatchet 3 Kg, Fibreglass Backboard Stretcher, Radio Walkie Sets 5 Watt, Blankets, Park Pickets, First Aid Kit, Twin Progned Graphel/Cat Hooks, Throw Bag, Gum Boots, Safety Goggles, Safety Helmet Water Rafting, Gps Sets, Navigation Lights, Maps, Charts And Compass, Chain Saw Machine, Camping Tent Water Resistant+ Mosquito Net, Inflatable Rescue Boat With 40 Hp Obm,
Integrated Security Surveillance System Service - Event Video Surveillance Public Safety Outdoor Perimeter Security Visitor Management Health Monitoring Solution For Cctv System Cctv Cameras; Recording Devices Capture Devices Usb; High Media Q..
Supply of 800 Electrical Safety Devices And Accessories Insulating Mats For Electrical Purposes As Per Is 15652 Q3
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 Shaft Seal Housing-Bottom, Parallel Pin A04x10, Safety Device B11.8X6.8, Hex Socket Screw Cm06x12, Retaining Ring 162/218Diax10, Shaft Seal Part Rsr350, Safety Device B20.8X13, Hex Socket Screw Cm12x20, Cover 190/292Diax35, Parallel Pin A08x16
Supply of Brushless Alternator 4.5 Kw Capacity, V-Belt Driven Suitable For Transom Mounting End 110V Dc, Train Lighting System As Per Rdso Specification Rdso/Pe/Spec/Tl/0054- 2003 Rev.-0 With Amdt. 1 And 2 With Scope Of Supply Includes: - A 4.5 Kw Alternator Complete With Alternator Pulley-01 No. B Rectifier Cum Regulator Unit- 01 No. C Deep Groove Axle Pulley-1 No. D Rubber Pad-02 Nos. E Safety Chain-02 Nos. F Suspension Hanger Pin Complete With Hardware-01 Set. G Belt Tensioning Device Complete As Per Rdso Drg. No. Skel-3940, Sheet 1 Alt-5 And Sheet 2 Alt-5- 1No.. Brushless Alternator 4.5 Kw Capacity, V-Belt Driven Suitable For Transom Mounting End 110V Dc, Tr Ain Lighting System As Per Rdso Specification Rdso/Pe/Spec/Tl/0054- 2003 Rev.-0 With Amdt. 1 And 2 With Scope Of Supply Includes: - A 4.5 Kw Alternator Complete With Alternator Pulley-01 No. B Rectifier Cum Regulato R Unit- 01 No. C Deep Groove Axle Pulley-1 No. D Rubber Pad-02 Nos. E Safety Chain-02 Nos. F Suspension Hanger Pin Complete With Hardware-01 Set. G Belt Tensioning Device Complete As Per Rdso Drg. No. Skel-394 0, Sheet 1 Alt-5 And Sheet 2 Alt-5- 1No. Warranty Period: 30 Months After The Date Of Delivery
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