Bids Are invited for Ultrasound Therapy Unit With Accessories - Equipment Type: Therapeutic Ultrasound Therapy Unit. , Operating Frequency: Dual Frequency – 1 Mhz And 3 Mhz. , Frequency Selection: User Selectable Through The Control Panel. , Therapy
Tender Overview
Project Description
Bids Are invited for Ultrasound Therapy Unit With Accessories - Equipment Type: Therapeutic Ultrasound Therapy Unit. , Operating Frequency: Dual Frequency – 1 Mhz And 3 Mhz. , Frequency Selection: User Selectable Through The Control Panel. , Therapy Modes: Continuous And Pulsed Modes. , Pulsed Operation: Multiple Selectable Duty Cycles, Preferably From 10% To 90% Or Better. , Pulse Repetition Frequency: Selectable Pulse Rates Including Approximately 16 Hz, 48 Hz And 100 Hz, Or Equivalent Clinically Suitable Settings. , Output Intensity In Pulsed Mode: Adjustable From Approximately 0.1 To 3.0 W/Cm² Or Better. , Output Intensity In Continuous Mode: Adjustable From Approximately 0.1 To 2.0 W/Cm² Or Better. , Effective Radiating Area (Era): Approximately 5 Cm² Or Suitable Standard Treatment Area. , Optional Small Transducer: Provision For Approximately 1 Cm² Era Transducer, Where Applicable. , Treatment Transducer: Ergonomically Designed And Suitable For Repeated Clinical Use. , Contact Sensing: Transducer Shall Have Patient/Treatment Contact Sensing Facility With Suitable Indication/Control. , Static Treatment Probe: Provision For Static Ultrasound Treatment Transducer/Probe, Where Applicable. , Beam Type: Controlled/Collimated Therapeutic Ultrasound Beam. , Beam Non-Uniformity Ratio (Bnr): ≤ 5.1:1 Or Better. , Treatment Timer: Adjustable Timer, Preferably 1–99 Minutes Or Better. , Display: Colour Tft/Lcd Touchscreen Or Equivalent Display Of Approximately 7 Inches Or Larger. , Display Information: Treatment Frequency, Mode, Intensity, Timer, Pulse Parameters And Other Relevant Treatment Parameters. , Preset Programs: Built-In Clinically Relevant Preset Treatment Programs May Be Provided. , User Memory: Minimum 30 User-Programmable/User-Defined Memory Locations Or Better. , Intensity Indication: Output Intensity Shall Be Displayed In Appropriate Units Such As W/Cm². , Transducer: Water-Resistant/Washable Transducer Suitable For Clinical Physiotherapy Use. , Control: Microprocessor-Controlled Operation With User-Friendly Interface. , Safety Features: Output Shall Be Automatically Controlled/Reduced/Stopped In Case Of Inadequate Transducer-Patient Contact Or Unsafe Operating Condition. , Mains Supply: 100–240 V Ac, 50/60 Hz, Or Suitable Universal Input. , Electrical Safety: Shall Comply With Applicable Medical Electrical Equipment Safety Requirements. , Applied Part: Type Bf Or Better, As Applicable. , Construction: Compact, Robust And Suitable For Hospital/Clinical Use. , The Equipment Shall Comply With The Latest Applicable Edition Of Iec 60601-1 & Iec 60601-2-5 Approved Certificates. , Quoted Model Should Comply With Ce/Us Fda & Iso 13485 Approved Certificates. , The Equipment Shall Have Appropriate Electrical Safety Classification And Protection Against Electric Shock. , The Bidder/Oem Shall Submit Valid Conformity Certificates, Test Reports And/Or Declarations For Applicable Standards Along With The Technical Bid. , All Applicable Statutory And Regulatory Requirements For Medical Devices/Equipment In India Shall Be Complied With. , Standard Ultrasound Therapy Transducer – 1 No. , Small-Area Transducer/Probe, Approximately 1 Cm² Era – Preferably 1 No. , Transducer Connecting Cable – 1 No., If Detachable. , Ultrasound Coupling Gel – Adequate Quantity For Initial Use. , Power Supply/Power Cord – 1 No. , Static Treatment Probe, If Required For The Quoted Configuration. , All Other Standard Accessories Required For Safe And Complete Operation.
BOQ
| Sl. No. | Item Title | Item Description |
| 1 | Equipment type: Therapeutic Ultrasound Therapy Unit. | Equipment type: Therapeutic Ultrasound Therapy Unit. |
| 2 | Operating frequency: Dual frequency – 1 MHz and 3 MHz. | Operating frequency: Dual frequency – 1 MHz and 3 MHz. |
| 3 | Frequency selection: User selectable through the control panel. | Frequency selection: User selectable through the control panel. |
| 4 | Therapy modes: Continuous and Pulsed modes. | Therapy modes: Continuous and Pulsed modes. |
| 5 | Pulsed operation: Multiple selectable duty cycles, preferably from 10% to 90% or better. | Pulsed operation: Multiple selectable duty cycles, preferably from 10% to 90% or better. |
| 6 | Pulse repetition frequency: Selectable pulse rates including approximately 16 Hz, 48 Hz and 100 Hz, or equivalent clinically suitable settings. | Pulse repetition frequency: Selectable pulse rates including approximately 16 Hz, 48 Hz and 100 Hz, or equivalent clinically suitable settings. |
| 7 | Output intensity in pulsed mode: Adjustable from approximately 0.1 to 3.0 W/cm² or better. | Output intensity in pulsed mode: Adjustable from approximately 0.1 to 3.0 W/cm² or better. |
| 8 | Output intensity in continuous mode: Adjustable from approximately 0.1 to 2.0 W/cm² or better. | Output intensity in continuous mode: Adjustable from approximately 0.1 to 2.0 W/cm² or better. |
| 9 | Effective Radiating Area (ERA): Approximately 5 cm² or suitable standard treatment area. | Effective Radiating Area (ERA): Approximately 5 cm² or suitable standard treatment area. |
| 10 | Optional small transducer: Provision for approximately 1 cm² ERA transducer, where applicable. | Optional small transducer: Provision for approximately 1 cm² ERA transducer, where applicable. |
| 11 | Treatment transducer: Ergonomically designed and suitable for repeated clinical use. | Treatment transducer: Ergonomically designed and suitable for repeated clinical use. |
| 12 | Contact sensing: Transducer shall have patient/treatment contact sensing facility with suitable indication/control. | Contact sensing: Transducer shall have patient/treatment contact sensing facility with suitable indication/control. |
| 13 | Static treatment probe: Provision for static ultrasound treatment transducer/probe, where applicable. | Static treatment probe: Provision for static ultrasound treatment transducer/probe, where applicable. |
| 14 | Beam type: Controlled/collimated therapeutic ultrasound beam. | Beam type: Controlled/collimated therapeutic ultrasound beam. |
| 15 | Beam Non-Uniformity Ratio (BNR): ≤ 5.1:1 or better. | Beam Non-Uniformity Ratio (BNR): ≤ 5.1:1 or better. |
| 16 | Treatment timer: Adjustable timer, preferably 1–99 minutes or better. | Treatment timer: Adjustable timer, preferably 1–99 minutes or better. |
| 17 | Display: Colour TFT/LCD touchscreen or equivalent display of approximately 7 inches or larger. | Display: Colour TFT/LCD touchscreen or equivalent display of approximately 7 inches or larger. |
| 18 | Display information: Treatment frequency, mode, intensity, timer, pulse parameters and other relevant treatment parameters. | Display information: Treatment frequency, mode, intensity, timer, pulse parameters and other relevant treatment parameters. |
| 19 | Preset programs: Built-in clinically relevant preset treatment programs may be provided. | Preset programs: Built-in clinically relevant preset treatment programs may be provided. |
| 20 | User memory: Minimum 30 user-programmable/user-defined memory locations or better. | User memory: Minimum 30 user-programmable/user-defined memory locations or better. |
| 21 | Intensity indication: Output intensity shall be displayed in appropriate units such as W/cm². | Intensity indication: Output intensity shall be displayed in appropriate units such as W/cm². |
| 22 | Transducer: Water-resistant/washable transducer suitable for clinical physiotherapy use. | Transducer: Water-resistant/washable transducer suitable for clinical physiotherapy use. |
| 23 | Control: Microprocessor-controlled operation with user-friendly interface. | Control: Microprocessor-controlled operation with user-friendly interface. |
| 24 | Safety features: Output shall be automatically controlled/reduced/stopped in case of inadequate transducer-patient contact or unsafe operating condition. | Safety features: Output shall be automatically controlled/reduced/stopped in case of inadequate transducer-patient contact or unsafe operating condition. |
| 25 | Mains supply: 100–240 V AC, 50/60 Hz, or suitable universal input. | Mains supply: 100–240 V AC, 50/60 Hz, or suitable universal input. |
| 26 | Electrical safety: Shall comply with applicable medical electrical equipment safety requirements. | Electrical safety: Shall comply with applicable medical electrical equipment safety requirements. |
| 27 | Applied part: Type BF or better, as applicable. | Applied part: Type BF or better, as applicable. |
| 28 | Construction: Compact, robust and suitable for hospital/clinical use. | Construction: Compact, robust and suitable for hospital/clinical use. |
| 29 | The equipment shall comply with the latest applicable edition of IEC 60601-1 & IEC 60601-2-5 approved certificates. | The equipment shall comply with the latest applicable edition of IEC 60601-1 & IEC 60601-2-5 approved certificates. |
| 30 | Quoted model should comply with CE/US FDA & ISO 13485 approved certificates. | Quoted model should comply with CE/US FDA & ISO 13485 approved certificates. |
| 31 | The equipment shall have appropriate electrical safety classification and protection against electric shock. | The equipment shall have appropriate electrical safety classification and protection against electric shock. |
| 32 | The bidder/OEM shall submit valid conformity certificates, test reports and/or declarations for applicable standards along with the technical bid. | The bidder/OEM shall submit valid conformity certificates, test reports and/or declarations for applicable standards along with the technical bid. |
| 33 | All applicable statutory and regulatory requirements for medical devices/equipment in India shall be complied with. | All applicable statutory and regulatory requirements for medical devices/equipment in India shall be complied with. |
| 34 | Standard ultrasound therapy transducer – 1 No. | Standard ultrasound therapy transducer – 1 No. |
| 35 | Small-area transducer/probe, approximately 1 cm² ERA – preferably 1 No. | Small-area transducer/probe, approximately 1 cm² ERA – preferably 1 No. |
| 36 | Transducer connecting cable – 1 No., if detachable. | Transducer connecting cable – 1 No., if detachable. |
| 37 | Ultrasound coupling gel – adequate quantity for initial use. | Ultrasound coupling gel – adequate quantity for initial use. |
| 38 | Power supply/power cord – 1 No. | Power supply/power cord – 1 No. |
| 39 | Static treatment probe, if required for the quoted configuration. | Static treatment probe, if required for the quoted configuration. |
| 40 | All other standard accessories required for safe and complete operation. | All other standard accessories required for safe and complete operation. |
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Tender Published
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Online submission via eProcurement portal.
Upcoming · 18 daysBid Opening Date
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