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| 1 | Physiotherapy Equipments |
| 2 | 1. Robtic Scanning laser• Device must have operating wave length of 1064mm,Power should be atleast 30w with possibility of adjustment from 0.5 to 30 watts in steps of 0.1 w with beam divergence of 35 degrees, Should have operating wavelength of 1064 nm , Should have hand probe for manual operation using main unit or through attaching hand free scanning system , Should have visible beam of 600 nm- 650nm with maximum output power of 5w.Should have – continuous wave.Pulsed wave Super pulse,Triangular modulated pulse Sequential and single phase .Frequency 1- 20,000 Hz. The dosage should be adjustable form 1- 200 J/cm2 .Hand probe – from 1-500cm2 with hand probe and up to 1200 cm 2 with scanner system. During single pulse operation the pulse power should be vary from 0.5 to 30w with pulse duration of 2-2000ms.Should have more than 35 pre- programme with body part navigation system .Should have 500-1000 memory positions with option to modify and defect them .Main supply 230v/50-60Hz, 115v/50-60Hz Should have built in encyclopedia with pictures .Should have adjustable spot size from 10 to 30mm when using hand probe Should have safety goggles ( eyewear) 2 Nos. with OD of 5 Should have LED colour touch screen for the main unit for and the scanner system of at least 8 inches screen size ( for scanning system screen size – 7 inches or more ).Should have portable main unit & light weight . Scanner system should have trolley with wheels .Should have European CE/ International standards certification. Maximum input power required by device approximate 160 VA .Should have fuses of type 2× T2AH /250 V according to IEC 60 Hz. Should have high quality metal /plastic trolley with castor wheels from same manufacturer with 4-5 drawers for keeping accessories.Should have degree of protection IP20 according to EN 60529.Power switch ( On /off) of IEC 60601 -1 standards |
| 3 | Cryotheraphy System• The unit should have 7.0\" TFT LED backlight with capacitive touch panel• The device must provide air flow of max 1000 liters/minute• Operating Air temperature must be up to -35 degrees Celsius• Maximum air pressure at output nozzle should be 50 mmHg• The unit should have dynamic as well as hands-free operation• The Unit should be supplied with the standard hose with 3 sizes of nozzles for different anatomic sites i.e. 5 mm, 10 mm & 15 mm diameter and angled nozzle• Option of flat stream nozzle should be available• The device should have option for therapy arm support holder• The device should be supplied with different types of sleeves: Elbow, Ankle, Conical, Flat, Ring, Leg and single sleeve and double sleeve adaptor• It must also have an option of lightweight hose with Focusing tip, Small, Medium & laser probe clamp• Airflow can be adjusted in the range of 1-9 levels.• Duration of therapy must be in the range of 1-99 minutes• Modes of operation should be continuous and Pulsed airflow• The device must be supplied with built in Trolley with castors• Mains supply 100-240 V, 50-60 Hz• Should be European CE certified / International Quality controls |
| 4 | Foccussrd Shock Wave Therapy Unit• Should be operating with single piezo electrical crystal & Electro acoustic lens. • Max frequency should be 25 H2.• Operating pressure – Energy flux Density 0.65 mg/mm square.• Optimal focal zone size of 5×35mm.• Should have built-in therapeutic encyclopedia with description, images & application of all pre programmed treatments (at least 25 preprogrammes).• Self identification of accessories & maintenance check.• Applicator should give at least 3 million shocks.• Penetration depth should be up to 65mm with coupling pads of sizes 0-35mm, 15-50mm, 30-65mm.• Applicator display should show number of shocks with intensity. • Screen size must be 8 inches at least.• Should have touch screen display on applicator hand piece.• Should have Trolley with castors & drawers for accessories.• Quality – International standards/ European CE.• Colour Touch screen interface• 2 different applicators• TD 20 for Large group of muscles• TD 15 for small group of muscles• Shock intensity – 1.0-5.0 Bar• Shock frequency – 1-20 Hz• Therapy period – 0-9999 shock |
| 5 | TECAR : Targeted Radio Frequency Therapy• Should have built-in feedback and safety features, • Should have preset protocols, user therapeutic protocols patient database.• More than 8 inches colour touch screen • Max power 230 w• Operating frequency 480-500 KHz• Different size of electrodes capacitive electrodes (20 mm-30-50-70mm ) resistive electrodes (20mm-30-50-70mm ) neutral electrode metallic 160*200mm • Should have 4 capacitive applicator Resistive applicator, 4 capacitive electordes 4 Resistive electrodes 1 neutral electrodes & cables• Should have trolley with wheels & shelves for storage space • Main 100 -240 V 50-60 H2• CE certified/ international Quality control• Hands free (Static) with adhesive electrodes• Therapy mode : Continuous & pulsed |
| 6 | Cardio Pulmonary Assessment• Should acquire 12 lead ECG simultaneously & display the same on screen with breadth by breadth pulmonary activity.• Should have integrated 12 lead exercise ECG with full disclosure & scroll back option during exercise test.• Should have software for ECG analysis with measurement & interpretation. • Should have facility to assess the risk of sudden cardiac death.• Should have facility for automatic arrhythmic defection.• Should have facility to test Breath by Breath ergo Spiro.• Should display date & charts their standard 9 panel Wasserman plot. • Should have real time acquisition and capturing of dynamic flow volume for End expiratory volume loops for evaluation of ventilatory limitation.• Should have facility for defection of AT & RCP automatically at the end of test.• Complete system should be from same manufacturer including Ergo Spiro system, should be able to measure both cardiac & pulmonary activities simultaneously.• Should have facility for multiple ventilatory threshold detection analysis. System should allow for post editing for threshold calculations AT1/VT1.• Calibration gas cylinder 6 litre – 1 no.• Thermo Hygrometer – 1 no.• BP monitor with adult cuff – 1 no.• Flow sensor dead space should be = 39ml.• Flow meter should not have any rotating parts or moving parts. • AT2/VT2, VO2 max, VCO2 max, VE/VCO2 slop and other parameters should have light weight pneumotach sensor based on variable orifice which meet ATs/ERS requirements.• Should have fast response and durable O2 technology for measuring O2 and fast infra red& electro chemical cell.• System should have heavy duty noiseless bicycle having digital display for load and speed.• System should have facility to connect external NIBP monitor which should take NIBP automatically as per set internal. • Main unit with complete PC, Printer, Heavy duty noiseless bicycle, stabilizer servo – 1 no.• Seal tight mask (large, medium) – 1 no. each. Chest electrodes – 100 nos.• System should be CE/European from notified body. • Pneumotech sensor – 1 no. |
| 7 | Vacuum Unit• Both the channels should be independent.• Should have continuous & pulse mode with pulse mode of 5, 10, 15 & 20 pulses/per minute.• Should have 60mm suction cups & electrodes & should have option for 30mm & 90mm suction cup electrodes and sponges. • Should have different programmes for pulsating modes. |
| 8 | KINVENT Wireless Biomechanical Measurement & Rehabilitation System1. System Overview• All components must connect via Bluetooth Low Energy (BLE 5.1 or higher).• Compatible with Android (6.0+) and iOS (11.0+) devices with minimum 2 GB RAM.• The mobile or tablet app should support:• Creation of individual athlete/patient profiles.• Real-time feedback during testing and training.• Standardized testing protocols for sports and rehabilitation.• Multi-sensor connectivity and cloud data synchronization.• Data export in PDF, CSV, and Excel formats.2. Components and Specifications• Hand Grip Strength Sensor• Measures peak and average isometric grip strength.• Max Force: ≥90 kg, Accuracy: ±0.1 kg or better.• Sampling Frequency: 1000 Hz.• Battery Life: ≥12 hours, Wireless Range: ≥40 m.• Handheld Push Dynamometer• For isometric strength testing of major muscle groups.• Max Force: ≥90 kg, Accuracy: ±0.1 kg or better.• Sampling Frequency: 1000 Hz.• Battery Life: ≥12 hours, Wireless Range: ≥40 m.• Pull Dynamometer• For fixed-position or chain-based strength assessment.• Max Force: ≥300 kg, Accuracy: Class C3 (<0.1%).• Frequency: 1000 Hz.• Battery Life: ≥12 hours, Wireless Range: ≥40 m.• Pneumatic Pressure Sensor (Bubble Type)• Measures pressure variations during pneumatic or inflatable exercises.• Max Pressure: 0.4 bar (5.8 psi), Accuracy: <1.5%.• Frequency: ≥100 Hz.• Compact, disinfectable housing suitable for clinical use.• Digital Goniometer / Motion Sensor• Measures joint range of motion (ROM) using inertial measurement (IMU).• Static Accuracy: ±2°, Dynamic Accuracy: ±7°.• Sampling Frequency: ≥400 Hz.• Battery Life: ≥12 hours, Wireless Range: ≥50 m.• Force Plates (Basic)• Dual-plate design for balance, stability, and jump testing.• Max Load: ≥600 kg per plate, Accuracy: ±0.1 kg.• Frequency: ≥1000 Hz.• Battery Life: ≥20 hours, Wireless Range: ≥20 m.3. General Technical & Safety Requirements• Auto sleep after 10 minutes of inactivity.• Rechargeable Li-Po batteries with medical-grade USB charger.• Easy disinfection using 70% alcohol wipes.• Fully wireless and portable system for lab or field use.• Compliant with the following standards:• IEC 60601-1 (Medical electrical equipment safety)• CE / FCC certification• ISO 15223, WEEE, RoHS compliance4. Additional Requirements• Should include centralized software for all sensors under a single application.• The software should allow customized testing protocols, real-time data visualization, and athlete performance reporting.• Cloud-based account management and multi-device data sync support.• Multi-sensor analytics dashboard for team or institutional monitoring.Additional Components • Grip Accessory (Size L)• Ergonomic detachable accessory for hand grip strength devices.• Designed for larger hand sizes to ensure standardized positioning and comfort during repeated trials.• Durable, washable, and disinfectable material suitable for clinical and sports settings.• Compatible with the system’s wireless grip strength sensor.• Reusable and compliant with medical hygiene standards (ISO 15223, RoHS). |
| 9 | ICE MACHINE• Category : commercial ice cube machine• Ice type: Diced / cube ice (approx. 17 g per cube)• Produces a reliable 100 kg of ice per 24 h• Stainless steel construction, hygienic, durable• Automatic start/stop, easy cleaning• Ice production (24 h) - 100 kg/day -At rated ambient and inlet water conditions • Storage (bin) capacity =60 kg • Ice cube weight / size ~17 g / cube Diced / cube type• Cooling system- Air-cooled -Simpler, lower maintenance (vswater-cooled) • Rated voltage / frequency / phase 230 V, 50 Hz, Single Phase• Power input / consumption ~ 850 W• Net weight ~ 74 kg • Dimensions (W × D × H) 735 × 603 × 1007 mm• Inlet water temperature +15 °C • Refrigerant / coolant- Needs to comply with safety and environmental norms• Material / Construction SUS Stainless Steel body & internal surfaces• For hygiene, corrosion resistance, durability |
| 10 | MASSAGE GUN MACHINE• Weight: 2.6 lbs• Size: 8 x 2.5 x 10.4 in• Battery life: 3 hours• Speed: 5 speeds of percussion• Motor: Brushless high-torque 90W motor• Power: Equipped with a 90W brushless high-torque motor.• Amplitude : Provides an amplitude of 14 millimeters, enabling the deepest muscle penetration for intensive therapy sessions• RPM: Features five adjustable speed settings, ranging from 1,700 to 2,700 PPM, allowing for customized therapy intensity• Battery Life: Provides up to 3 hours of use per charge with its rechargeable lithium-ion battery.• Bluetooth®: Connects via Bluetooth (for automated speed control)• Pressure sensor: Patented Pressure Sensor Technology™ showcases how much pressure is being applied• TSA approved: Approved by TSA for carry-on• Head attachments: 5 (fork, ball, cushion, flat, bullet)• Components :The actual device, Power supply + adapters• Head attachments (5) |
| 11 | BODYCOMPOSITION ANALYZER MACHINE1. Measurement Method : Direct Segmental Multi- frequency Bioelectrical Impedance Analysis Method(DSM- BIA ) and Simultaneous Multi- frequency Impedance Measurement (SMFIM) using Tetra-polar electrode method using 8 touch electrodes2. Multi- frequency FrequencyRange:5,50,250kHz.3. Measurement Area : Simultaneous Multi- frequency Impedance Measurement (SMF-BIA)Whole Body and Segmental Measurement(Right Arm, Left Arm, Trunk, Right Leg,andLeft Leg)4. Result Sheet Dataforadults: Results and Interpretations5. Body Composition Analysis (Total Body Water, Protein, Minerals,Body Fat Mass, Weight), Muscle-Fat Analysis (Weight, Skeletal Muscle Mass, Body Fat Mass),Obesity Analysis (Body Mass Index, Percent Body Fat),Segmental Lean Analysis (Right Arm, Left Arm, Trunk,Right Leg, Left Leg), Segmental Fat Analysis (Right Arm, Left Arm, Trunk, Right Leg, Left Leg) Body Composition History (Weight, SkeletalMuscle Mass, Percent Body Fat) Weight Control(Target Weight,Weight Control, Fat Control,Muscle Control), Nutrition Evaluation (Protein, Minerals, Fat Mass), Obesity Evaluation (BMI, Percent Body Fat), Body Balance Evaluation (Upper,Lower, Upper-Lower), Waist-HipRatio (Graph), Visceral Fat Level (Graph), Research Parameters (Skeletal MuscleMass, Fat Free Mass, BasalMetabolicRate, Waist- Hip Ratio, Waist Circumference, VisceralFat Level, Obesity Degree, Recommended calorie intake per day,Calorie Expenditure of Exercise,Blood Pressure (Systolic, Diastolic,Pulse, Mean Artery Pressure,Pulse Pressure, Rate Pressure Product)) Results Interpretation QR Code Impedance (Each segment and each frequency)6. Optional Equipment attachments :Stadiometerfrom same OEM, Blood pressure monitor from same OEM, Thermal printer from OEM, Hand Grip Dynamometer.7. Touch Screen: Touch Screen sensor location adjustable8. Printing Logo: Printing the hospitalname, address, contact information, and logo available.9. Data Storage Upto100,000 dataunitscan be stored whenusingan ID10. Measurement Mode : Scale Mode, Body Composition Mode11. VariousResult Sheets : Test ResultsSheet, Test Results Sheet for Children12. Checking Measurement Results: LCD Monitor, internet13. Measurement Current : Approx.180µA ±1514. Power Input AC100-240V,50-60Hz,1.4-0.7A15. PowerOutput DC 12V, 5.0A,60W MAX16. Display:7inch wide ColorLCD having both Touchscreen and Keypad option.17. Transmission Device : 5USB port 2RS- 232C 4EA,Bluetooth, Wi-Fi18. PrintingDevice: USB port (printer designated by the manufacturer), thermalprinter (optional), Machine should be supplied along with compatible printer.19. Dimensions : Dimension Main Unit 641*436*1029mm(W*D*H+10mm)a. Main Unit +Height Meter 795*436*2327mm(W× S*H+10mm20. Product Weight : Approx.18kga. (mainunit)21. Measurement Time:Approx. 30 sec.22. Measurement Height : 100~ 220 cm23. Measurement Weight : 10 ~ 250 kg24. ApplicableAge:3~99years25. Operating Environment : 5~ 40°C,15~93 %RH (no condensation)26. Storage Environment : 25~ 70°C,10~80%RH,50~106 kPa (No Condensation)27. USB Storage : Backup data should be saved in the software by using a USB Thumb Drive having the option to restoreresults on the softwarefrom a backup file.28. QRCode:Scan the QR codeon the LCD or result sheet, transmit it toa. The management website, and check the results.b. Remote Support :Remote Technical Support with PC 29. CERTIFICATES: The system shouldhave US-FDAregistered, EuropeanCE and EN-ISO certification |
| 12 | PRP Preparation System with UPS and PRP Kit1. Centrifuge machine Swing out Rotor – S - 650Maximum speed RPH – 4500Max RCF(g) – 35302. PRP Kits – • It should be capable of processing 25-50ml of blood.• PRP concentrate 6-8 *higher than baseline RBC, Plasma and PRP should be isolated separately PRP kit should be capable of adjusting precise volume of PRP.• Kit should be capable of producing true.• LPPRP with an advanced leukocyte depletion filler. • PRP kit should be compatible with different classical centrifuges.• Kit should contain basic accessories like ACD- A, scalp vein set and lure lock syringes for aspiration and infection. • ACD supplied should be from clinical grade and not for diagnostic purposes.• Customizable 1-5 ml PRP volume without affecting the platelet concentration.• 100% closed and sterile system.• US patented technology.• Kit should be made in India.• The kit should be provided as per the requirement for sports medicine centre. |
| 13 | Portable Ultasound Machine• Should be a diagnostic Musculoskeletal Ultrasound Machine• Complete with preset & measurement for sports Medicine application, musculoskeletal imaging, general imaging, vascular small parts, thyroid, and CEUS with quantification tool fully integrated in main unit to measure wi/ wo curves and intensity against time packages.• System should be of latest technology with Windows 10 OS or better based platform• Rotatable keyboard with height adjustment, should include alphanumeric keyboard with min 10” colour LCD touch screen for accession functions• Tiltable 21.5” or higher medical grade display Monitor with articulating arm• Should have 4 active pin less probes connectors• Should have 2D frame rate of minimum 6000 or higher frames per sec• Should have colourdoppler frame rate of 400 Hz or more• Should have minimum 256 or higher gray levels• Should have dynamic range of 350dB or higher• Archiving capabilities with sorting of clips and still images in SSD storage• Internal SSD storage with minimum of 500 GB or higher• B-Mode/ Dual –B Mode/ M-Mode• PW/ HPRF Doppler• Colour Doppler and power Doppler• Speckle reduction software• Should have post processing from stored data• Should have follow-up option for comparison of post and pre surgery with different modality like MRI/ CT or same modality• Speed of sound regulation- possibility to modify the speed of value in order to focalization on the lateral direction• Bi-raid and Tri-raids• Should have panoramic imaging of minimum 60 cm or higher with CFM• Ultra sensitivity colour Doppler to pick up small vessels and slow flow detections• Unlimited users preset for all applications• System imaging capable from 1 to min 22Mhz or higher frequency for superficial imaging applications• Should have radio frequency based intima media thickness measurement• Should have radio frequency based arterial stiffness measurements• Should have strain based Elastography in linear array & convex array probes• Should have quantification tools fully loaded in ultrasound for contrast study imaging with intensity curves• Should have option to upgrade to 2D shear-wave elastography in convex probes• Should supply an online UPS with minimum 30 minutes back up• Should supply a colour Ink – jet printer• Should have DICOM, USB, HDMi output in main unit• System should have CE and US-FDA certification• Standard transducer to be offered and the rate shall be quoted separately which will be considered for L1 evalution.a) Convex array transducer with bandwidth frequency of (1.0 to 8.0 MHz) with General imaging application with min 44cm Depth or higher with strain based elastography imagingb) L-shape linear array transducer with bandwidth frequency of (6.0 to 18.0 MHz) for vascular access, small parts, MSK & sports medicine imaging application with strain based elastography imagingc) Linear array transducer with bandwidth frequency of (4.0 to 15.0 MHz) for vascular access, small parts, Breast, MSK, Thyroid imaging application with strain based elastography imagingLinear transducer with bandwidth frequency of (3.0 to 11.0 MHz)for small parts, MSK and vascular access imaging application |
| 14 | Autoclave Machine• Stainless steel Autoclave• Autoclave portable stainless steel six wing nut type• (sterilizer Dressing Pressure Type)• size capacity 21 litre to 39 litre• Seam weid construction ensures bacteria free environment.The unit is made of stainless steel.Ring is made of Aluminium.Lid is made of stainless steel combined with Aluminium.The unit is equipped with pressure guage, safety valve, steam release valve, vaccum release valve, Rubber Gasket container, inner tripod stand and mild steel stand for autoclave.Model• LRS 011 12*12 inch • capacity 21 litres• variants non electrical /electrical Please Enable Macros to View BoQ information |