Physiotherapy Equipment 2026 IIIrd Call

Treatment Couch Examination, manipulation, and treatment table, hydraulic or electric height adjustment by means of a low voltage (24V) foot switch or with foot rail. The couch has four movable sections: the leg/back section and the head section can be adjusted by using a gas spring assisted system. The couch can be set in "partial trendelenburg" and "sitting" positions, even with the patient on it. The head section, equipped with an elongated breathing hole, can be adjusted both in positive and in negative positions. Fully adjustable (height) side section arms. Number of sections: 5, Max safety load (kg): 200, Height adjustment: Electric/hydraulic, Min / max table height (cm): 47-97, Mains supply: 220V 50-60Hz / 24V 70VA, Actuator thrust (N): 6000, IP Protection: 54, Head section adjustment: Gas spring-assisted, Head section tilt: +85° -35°, Wheels diameter (mm) :65, Braking system: Central, Upholstery safety rating: 1 IM, Padding thickness (mm): 40 Density (kg/m³): 30, Weight (kg): 82, Should have -This is an electric height adjustment system that can be reached from anywhere around the table, without having to locate the foot switch. It is activated by simply pressing or lifting the perimeter, CE European /FDA /ISO certification, 2-year warranty

High Performance laser Technical Specification, 01. Color Touch LCD Display – 17.8cm, 02. The unit should have Illustrated therapeutic encyclopedia, 03. The unit should have 4 channels attachment 04. The unit should have number of in bult program min 200 application adapter-1cm²,5cm², 05. Radiation mode- continuous, pulse and super pulse., 06. Duty cycle or pulse time setting., 07. Automatic treatment time calculation on the basis of treatment B16area., 08. Cooperation with scanning applicator, 09. unit mode – program mode/ manual mode, 10. Pilot beam- 5mW-660nm, 11. High power Peak output power- 18 W, 12. The unit supply with high power probe with cluster applicator 1800mW, 13. The unit should be in build program Class 4 & class 3b ‘, 14. Type of radiation- 808nm for 8W and 980nm for 10 W, 15. Energy dose- 05,-50J/cm², 16. Pulse frequency – 1-10000 Hz, 17. Duty factor- 1-90%, pulse, 18. The cluster applicator wavelength should be R 200mW + IR 1600mW, 19. The cluster power adjustment -50% 100%, 20. Thea cluster applicator duty factor in pules mode 1-5000 Hz , 21. Treatment time- max-100 min, 22. Min main supply- 230V,50-60Hz, 130W 150VA, 23. The unit screen showing all the attachment applicator at the treatment time, 24. The unit support optional scanning laser wavelength 808nm with maximum output 450mW and, Wavelength 606nm with maximum output power 100 mW,25. 26 preset treatment sequence for scanning laser, 26. Protective goggles – 2 pcs, 27. The unit certified from CDSECO and CE European/FDA USA, Trolley for the unit and accessories

Insole Material compatible with Podiatric Scanner The material Type: Custom-mouldable performance insole, The material Usage: High-impact court sports & daily support, Dimensions, • Top layer: polyester, • Enhances stiffness & stability, • Reduces energy loss at the metatarsophalangeal (MTP) joint, • Improves propulsion & energy return, • Supercritical Nitrogen Foam: High elasticity, responsive cushioning & energy return, • Balance Plate & bottom layer: polyester, • Lightweight EVA Foam: Durable, flexible & lightweight base cushioning for comfort, • Shock Absorber Inserts: Up to 90% impact absorption for superior shock protection • Thickness (Forefoot):2 mm, • Available Sizes: EU 36–48, • Weight: ~30 g, • Ultra-minimal design, • Suitable for slim-profile applications (e.g., smart tracking insoles), • Custom-moulded patented balance plate for dynamic arch support, • Enhanced shock absorption (heel & ball of foot), • High-strength base surface for durability, • Heel cushioning designed to follow natural gait, • Perforated forefoot area for ventilation & moisture control, • Antibacterial top layer coating, • The supplied material compatible with European standard equipment, • The supplied with international parameter and certified in EU

Radio frequency electromegnetic device 1. Should be able to give treatment in Capacitive and Resistive Energy Transfer (CET & RET) modes IASTM-for soft tissue mobilization Bipolar- Auto Mode, 2. Must have ability to operate in Pulsed and Continuous wave operation modes of emission, 3. Adjustable frequency range: 300 kHz- 500kHz-750kHs- 1.0MHz, 4. The power level adjustment range 0-10% step 0.5%, 0-40% step 1%, 0-30%-4%, 5. The unit work with four frequencies, 6. The unit indicator of the level of contact between the electrode and patient body, 7. The unit indicate the value of current flowing through the patient tissues, 8. Maximum output power: Up to 100 Watts or more, 9. Real-time impedance monitoring and auto-adjustment with built in sensor. 10. User friendly digital display interface of touchscreen colour display (5-10 inches)LCD/LED with clear visuals for the multi-function buttons, 11. Built-in clinical treatment protocols (minimum 10-50+) with 3D Database of present treatment sequences in the form of an encyclopedia with descriptions of the methodology and presentation of manual therapy techniques with patient movement, 12. Customizable user-defined program memory up to 100, 13. Internal integrated air-cooling system for thermal management and prevent machine overheating, 14. Universal voltage compatibility: 110-240V AC, 50-60 Hz ,15. CE, BIS, US FDA ISO 13485 and CDSCORegistration copy, 16. Emergency stop button included, 17. Visual and audio alarms for safety alerts and for errors: for improper use or contact loss, 18. Gradual soft start & stop energy application, 19. Should have both thermal and athermal option mode for treatment., 20. Operating modes: Unipolar, Bipolar, Neuro Dinamico, Static Automatic., 21. Accessories Supply with Dedicated Trolley with electrode heater and 3 Capacious drawers for Unit accessories and containerfor accessoriesand switch mode power supply for the Trolley, 22. Comprehensive warranty for 2 years with guarantee to made available the necessary spare parts as and when required., 23. Real-time monitoring of auto impedance, 24. Overheat protection with automatic shutoff, 25. Non-conductive ground electrode coating, 26. The Unit supply with IASTM Tool, 27. Dual electrode system: Capacitive and Resistive type, 28. Capacitive Electrode sizes: small to large (25 mm, 40 mm ,55 mm ,70 mm) 29. Resistive Electrode sizes: small to large (25 mm, 40 mm ,55 mm ,70 mm) 30. Convex resistive electrode 14mm and 40 mm, 31. IASTM applicator cable for RF current, 32. IASTM applicator cable and extension cord, 33. Passive electrode, 34. Angular applicator for active electrode 35. Straight applicator for active electrode 36. Elastic Velcro 40x10 cm,60x10 cm, 80x10 cm,100x10 cm

Podiatric scanner with insole maker • The unit should have interface integrated 24” Color touch screen, • The unit should have interactive Foot Balance 3D Scanning with analysis- and with software, • The Unit should have Scanning speed 5-15 s per phase with optimal connectivity, • The unit should have Scanning accuracy +/-1 mm for the foot size, benchmarked on plastic foot models, no need to remove socks to scan, • The Scanner is designer for normal environmental conditions; (a) Indoor use, (b) Altitude up to 2000m, (c) Temperature 5°C to 40°C, (d) Maximum relative humidity 80% for temperatures up to 31°C decreasing linearly to 50° relative humidity at 40°C, (e) Mains supply voltage fluctuations up to +/- 10% of the nominal voltag, (f) Temporary overvoltagesoccurring on the mains supply, (g) Applicable pollution degree 2, • The unit should be supplied with Power plug 10m cable (white) + adapter, • The unit should be Internet connection wired preferred (RJ45), Preferred 100+Mbps, min 10 Mbps, • The unit should have Wi-Fi intel Wi-Fi 6 AX201, • The bidder provides size recommendations in millimeters and US-, EU-, and UK sizes, • The device is Class 1 laser compliant, • The unit Dimensions (cm) 72 × 96 × 144, • The unit Weight (kg) 70 total, • The unit 60.5 (metal frame w/o electronics) • The unit supply 3 Sets of reinforcement, • The unit supply 100 pairs insoles for sports,medical,diabetic and formal insoles from size 28 to 52 all even number free with the machine, • The unit certified CE European / FDA approved

MICROWAVE DIATHERMY 1. The device should have 2-way applicator with angle adjustable reflector panels providing a gentle, warm sensation by covering the affected area. 2. The device should have “one touch of a button” easy use arm - The arm can be easily expanded and rotated by pressing (holding) the “Arm Lock Release Button.” Setting the position of the applicator is quick and easy to do. 3. The device should have Output restriction function for increased safety - Equipped with “Output Limit function” to prevent exceeding the preset output in case. 4. The device should have Mode switch function - Users can switch between continuous output and intermittent output. 5. The device should have Enhanced-visibility - Output level meters and digital treatment time display allow you to check the treatment status with one glance. 6. Continuous output mode: 125 W continuous (output control 5–125 W, 5 W increments) 7. Intermittent output mode: 200 W at peak/125 W average (average output control 5–125 W) 8. Working frequency should be 2450 MHz +/- 10 MHz 9. Therapy time should be 00:01 to 30:00 min 10. Approximate External Dimensionsshould be: 493(L) x 482(B) x 1174(H) mm. 11. Mains voltage: ~200 V to 240 V or ~100 V to 127 V 12. Frequency: 50 Hz to 60 Hz. 13. Should have Continual and pulsed mode. 14. Should be USFDA/ European CE Certified 15. Should have 2-year warranty

Multi-functional treatment unit 1. The unit should for adult and should be user friendly, 2. It should be with touching colour touch screen of minimum 5" in size with coloured display of all waveform as well as the numbers should be clearly visible from a distance of up to 4-5 feet, 3. The unit should be touchscreen as well with key button for operation, 4. The unit should be upgradable, 5. The unit is equipped with three fully independent treatment channels. The list of available therapies in particular channels is shown in the Table 6. The unit should have optional an internal battery which should least for 6 hours backup, 7. The unit should have encyclopaedia as per the with Medical filed, 8. The main unit should have reachable battery withoperating time of at least 120 minutes 9. The unit should have compatible with low intensitypulsed ultrasound mode and electrodiagnostic Parmeter. 10. The unit should have minimum 300 in buildtreatment programs. (a) Non - Invasive Therapeutic Device. 1- intended for carrying our treatment procedures using: bipolar (bidirectional) and unipolar (unidirectional) low frequency currents, 2- bipolar (bidirectional) and unipolar (unidirectional) medium frequency currents, 3- standard ultrasound therapy, low-intensity pulsed ultrasound (LIPUS) therapy and phonophoresis, 4- combination method of current and ultrasounds. Treatments are performed by direct contact method with non-injured skin. Parts of the body intended for treatments with , upper limbs (shoulder, arm, forearm, hand), lowerlimbs (hip, thigh, shank, foot), neck and face for interaction with body tissues such as muscle, skeletal, nervous system and/or skin. (b) information about available configurations 1. The unit have possesses the base of preset treatment procedures along with therapeutic encyclopaedia, which significantly increases comfort of operation. 2. The unit should be a possibility to create own userdefined: 3. It should have programs - for all therapies and all sequences - for electrotherapy. 4. The unit should be perform treatments by: 5. TENS, BURST and formed in packages to spastic paralysis SP-TENS currents, interferential currents - dynamic and isoplanar, one-channel sine wave current (AMF), Kotz' - Russian stimulation, diadynamic according to Bernard - Mf, DF, CP, CP-ISO, LP, RS, MM currents (in continuous and interrupted mode), ionophoresis and galvanization of constant current (in the continuous and interrupted mode), Talbert (Ultra Reiz), Leduc' and neofaradic (in continuous and interrupted mode), medium frequency current, unipolar and bipolar sine surge currents, triangular or rectangular pulses (in continuous and interrupted mode), microcurrents, 1G pulses, EMS currents, H-waves, exponential pulses, tonolysis and Hufschmidt stimulation - to spastic paralysis, qualitative and quantitative electrodiagnostic of the nervous-muscle system. 6. The unit should have supply with standard ultrasound head, which generates an ultrasound wave with a frequency of 1 MHz or 3 MHz, with a total area of the head front of 5 cm2, C) Technical Parameter — 1. Unit should have unipolar sine surge 30 mA 2. The unit should have galvanic, IG 80 mA 3. The unit should have Dia dynamic 70 mA 4. The Unit should have bipolar sine surge, Hufschmidt stimulation -100 mA 5. The unit should have interferential, TENS, Kotz's stimulation, pulse currents, MF -140mAThe unit should have tocolysis, EMS, H-waves, exponential pulses -140 mA microcurrents -1000 pA, max. voltage amplitude in the patient circuit (CV mode) 140 V 6. the unit should be continuous/ pulse emission mode 7. The US head should be water resistant heads with thermal effect 8. The unit should be supplying US head max. ultrasound intensity - 2/3 W/cm2 1&3 MHz 5cm 9. The unit US head frequency in pulse mode - 10 -150 Hz 10. The unit US head should be work in continuous/ pulse emission mode 11. The unit Supply with Lupus therapy program & head Lipus ultrasound head simultaneously total treatment area of head front 17.3 cm 12. The unit should have mains power supply 240 VAC, 50/60 Hz 13.CE EUR Regulation I USA FDA / As per Indian Norms CDSCO certified. 14.Electrical safety test report PN-EN-60601-1/EN-60601-1/IEC 60601-1 15.Original copy origin of certificate, 16. The unit Supply with standard accessories as per the catalogue & unit trolley 3 section (D) – optional Accessories 1.The unit should have optional attachment 2 dual frequency ultrasound treatment area - 1 & 3 5cm &1 cm 2. avidity optional accessories - with box point electrode with adapter 6mm,10mm,15mm, 20mm¬01set 3. The unit have optional - inbuild battery -voltage- 18V 2100 mAh 8 hours

Ortho traction unit 1. The device should be compatible or better than the below technical parameters: a. Power Input: 200 VA, b. External Dimensions: Approximately 800 x 1240 x 1840 (H) mm approx, c. Weight: Approximately 124 kg, d. Treatment Time: 1-99 minutes (adjustable in 1-minute increments) e. Safety Features: Patient stop switch, over-traction protection, f. Rated Power Supply: AC 110 V/220 V/230 V/240 V 50/60 Hz, 2. The approximate Traction Force of the device should be: a. Cervical: 29–245 N (3–25 kgf) b. Lumbar: 49–588 N (5–60 kgf) 3. The device should have: a. Automatic Traction Force Setting b. Auto-Fit Side Supports c. Inflatable Traction Belt d. Cervical Sling e. Head Weight Offset Function f. Inbuilt Coldness Reducing Heater g. Free Positionable Operation Panel h. Space-Saving Design 4. The device should automatically shifts from sitting to lying position. 5. The device should be 2 in 1 model for cervical & lumbar traction in a relaxed posture. 6. The device should be EU-CE certified.

Pneumatic cold therapy 1. The unit must have following feature 2. Should have Temperature of the treatment air: -30°C 3. Should use Room air to provide cool air without need of any consumable 4. Should have atleast 10 inches’ large display for ease of operation 5. Should have Pre-set program & Individual programming combining air flow & Treatment time 6. Should have Individual programming combining air flow & Treatment time for atleast 100 entries. 7. Should have adjustable Air flow levels 8. Should have Treatment Tube Length 250 cm or more for easy approach to different treatment areas 9. Should have TEST PROGRAM to control and measure all important functions, without opening the unit and without any measurement device. 10. Defrosting should be displayed on control Panel 11. Air filter should be easily approachable for cleaning and changing 12. Should have USB and RS232 interface for possible device communication for writing log files or for updates. 13. Should have Energy-saving eco standby operation 14. Treatment time should be adjustable up to 99 Min 15. Air outlet should pivot through 90° so you can reach all around the clinic 16. Should have Easy-access condensed water container 17. Medical device: Class IIa 18. Mains connection: 220-240 V / 50-60 Hz 19. Max. power consumption during therapy:: 1200 VA 20. Interface: USB 2.0, RS232 21. Fan levels: 1-9 22. Length of the treatment tube: 250 cm 23. Therapy time: 1:00 – 100:00 min 24. The device bears the CE mark in accordance with the EC directive on medical devices 93/42/EEC and meets the essential requirements of appendix I of this directive.