Health and Family Welfare Boards / Undertakings / PSU Closing in 18 days TDR #57356680

Bids Are invited for Low Level Laser Therapy Machine - System Type: Computerized Low-Level Therapeutic Laser / Photobiomodulation System With Programmable Treatment Parameters. , Laser Source: Semiconductor Therapeutic Laser Source(S), Such As Gaalas

Issued by Boards / Undertakings / PSU · Muzaffarpur, Bihar
Tender Value
Ref. Documents
Estimated cost
Bid Submission
25 Sep 2026
18 days left
EMD
1.10 Lakhs
Bank guarantee accepted
Document Fee
Ref. Documents
Non-refundable
Tender Type
Gem

Tender Overview

Competition Type
NCB
Bidding Type
Tender
Location / State
Muzaffarpur → Bihar
EMD Exemption
Available
Quantity
1

Project Description

Bids Are invited for Low Level Laser Therapy Machine - System Type: Computerized Low-Level Therapeutic Laser / Photobiomodulation System With Programmable Treatment Parameters. , Laser Source: Semiconductor Therapeutic Laser Source(S), Such As Gaalas Or Equivalent Technology, Suitable For Lllt/Photobiomodulation. , Operating Mode: Continuous And Pulsed Modes Shall Be Available. , Wavelength: At Least One Therapeutic Wavelength In The Red/Near-Infrared Range; System Shall Support Clinically Appropriate Wavelengths. Multiple Interchangeable Probes/Applicators May Be Offered. , Output Power: Variable/Programmable Therapeutic Output Power With Suitable Control Through The System Interface. The Offered Configuration Shall Provide Adequate Output For Intended Clinical Applications. , Pulse Frequency: Programmable Pulse Frequency Covering A Clinically Useful Range, Preferably Extending From Low-Frequency Operation To At Least Several Khz, As Applicable To The Offered System. , Treatment Time: Programmable Treatment Timer With A Minimum Range Of 0–60 Minutes Or Wider. , Treatment Parameter Control: User-Selectable Control Of Relevant Treatment Parameters Such As Wavelength/Probe, Output Power, Mode, Pulse Frequency And Treatment Time, As Applicable. , Display / User Interface: Colour Touchscreen Or Equivalent User-Friendly Display For Setting, Monitoring And Confirming Treatment Parameters. , Probe/Applicator Detection: Automatic Recognition/Detection Of Connected Therapeutic Probe(S)/Applicator(S) Is Preferred. , Treatment Indication / Preset: Programmable Or Preconfigured Treatment Protocols/Presets For Commonly Used Clinical Applications, With Facility For User-Defined Settings. , Memory: Patient/Treatment Parameter Storage Or User Memory Facility Is Preferred, With Access Control As Applicable. , Safety Features: Audible/Visual Indication Of Treatment Status And/Or Completion, Controlled Activation, Fault Indication, Emergency Stop Or Equivalent Safety Provision, And Protection Against Unintended Laser Emission. , Password/Access Control: User Access Control/Password Protection For Treatment Settings And Stored Data, Where Applicable. , Laser Safety Classification: The Complete System And Each Applicable Laser Source/Probe Shall Comply With The Applicable Laser Safety Classification And Standards. If Class 3B Laser Is Offered, Appropriate Safety Controls And Protective Eyewear Shall Be Supplied. , Electrical Safety: Suitable For Operation On 230 V Ac, 50 Hz Indian Mains Supply, With Appropriate Protection. Input Range May Be Universal (E.G. 100–240 V Ac, 50/60 Hz) Or Equivalent. , Construction: Compact, Robust And Easy-To-Clean Medical-Grade Housing Suitable For Hospital Use. , Portability: Bench-Top/Portable Configuration Preferred, With Provision For Safe Handling And Storage Of Probes/Accessories. , Cooling: Adequate Thermal Management/Cooling System To Ensure Safe And Stable Operation During Specified Duty Cycle. , Minimum Required Number Of Therapeutic Laser Probes/Applicators As Per Offered Configuration. , Protective Laser Safety Eyewear Appropriate To The Wavelength(S) And Laser Safety Class Supplied; Adequate Quantity For Operator And Patient. , Probe/Applicator Holder Or Stand, Where Applicable. , Power Cable And All Necessary Connection Cables. , Calibration/Test Facility Or Accessories Required For Routine Performance Verification, Where Applicable. , User/Operator Manual And Service/Maintenance Manual In English. , Any Other Accessories Necessary For Safe And Complete Operation Of The Quoted System. , The Offered Equipment Shall Comply With Applicable Indian Statutory Requirements And Applicable International Standards For Medical Electrical Equipment And Laser Safety. , The Bidder Shall Provide Valid Conformity/Safety Certificates Applicable To The Quoted Model, As Required Under Prevailing Indian Regulations And Procurement Conditions. , Laser Safety Eyewear Shall Be Supplied According To The Wavelength(S) Of The Offered Laser System And Shall Carry Appropriate Identification/Marking. , The Bidder Shall Clearly State The Laser Classification, Wavelength(S), Maximum Output Power And Relevant Safety Standard(S) In The Technical Offer. , Where Applicable, The Equipment Shall Comply With Iec 60825-1 Or The Latest Applicable Edition/Standard, Along With Applicable Medical Electrical Safety Requirements. , All Electrical Accessories Supplied With The System Shall Be Suitable For Indian Mains Supply And Hospital Use. , Quoted Model Should Comply With Ce/Us Fda, Iso 13485 & Iec 60601-2-22 Certificate.

BOQ

Sl. No. Item TitleItem Description
1System type: Computerized low-level therapeutic laser / photobiomodulation system with programmable treatment parameters.System type: Computerized low-level therapeutic laser / photobiomodulation system with programmable treatment parameters.
2Laser source: Semiconductor therapeutic laser source(s), such as GaAlAs or equivalent technology, suitable for LLLT/photobiomodulation.Laser source: Semiconductor therapeutic laser source(s), such as GaAlAs or equivalent technology, suitable for LLLT/photobiomodulation.
3Operating mode: Continuous and pulsed modes shall be available.Operating mode: Continuous and pulsed modes shall be available.
4Wavelength: At least one therapeutic wavelength in the red/near-infrared range; system shall support clinically appropriate wavelengths. Multiple interchangeable probes/applicators may be offered.Wavelength: At least one therapeutic wavelength in the red/near-infrared range; system shall support clinically appropriate wavelengths. Multiple interchangeable probes/applicators may be offered.
5Output power: Variable/programmable therapeutic output power with suitable control through the system interface. The offered configuration shall provide adequate output for intended clinical applications.Output power: Variable/programmable therapeutic output power with suitable control through the system interface. The offered configuration shall provide adequate output for intended clinical applications.
6Pulse frequency: Programmable pulse frequency covering a clinically useful range, preferably extending from low-frequency operation to at least several kHz, as applicable to the offered system.Pulse frequency: Programmable pulse frequency covering a clinically useful range, preferably extending from low-frequency operation to at least several kHz, as applicable to the offered system.
7Treatment time: Programmable treatment timer with a minimum range of 0–60 minutes or wider.Treatment time: Programmable treatment timer with a minimum range of 0–60 minutes or wider.
8Treatment parameter control: User-selectable control of relevant treatment parameters such as wavelength/probe, output power, mode, pulse frequency and treatment time, as applicable.Treatment parameter control: User-selectable control of relevant treatment parameters such as wavelength/probe, output power, mode, pulse frequency and treatment time, as applicable.
9Display / user interface: Colour touchscreen or equivalent user-friendly display for setting, monitoring and confirming treatment parameters.Display / user interface: Colour touchscreen or equivalent user-friendly display for setting, monitoring and confirming treatment parameters.
10Probe/applicator detection: Automatic recognition/detection of connected therapeutic probe(s)/applicator(s) is preferred.Probe/applicator detection: Automatic recognition/detection of connected therapeutic probe(s)/applicator(s) is preferred.
11Treatment indication / preset: Programmable or preconfigured treatment protocols/presets for commonly used clinical applications, with facility for user-defined settings.Treatment indication / preset: Programmable or preconfigured treatment protocols/presets for commonly used clinical applications, with facility for user-defined settings.
12Memory: Patient/treatment parameter storage or user memory facility is preferred, with access control as applicable.Memory: Patient/treatment parameter storage or user memory facility is preferred, with access control as applicable.
13Safety features: Audible/visual indication of treatment status and/or completion, controlled activation, fault indication, emergency stop or equivalent safety provision, and protection against unintended laser emission.Safety features: Audible/visual indication of treatment status and/or completion, controlled activation, fault indication, emergency stop or equivalent safety provision, and protection against unintended laser emission.
14Password/access control: User access control/password protection for treatment settings and stored data, where applicable.Password/access control: User access control/password protection for treatment settings and stored data, where applicable.
15Laser safety classification: The complete system and each applicable laser source/probe shall comply with the applicable laser safety classification and standards. If Class 3B laser is offered, appropriate safety controls and protective eyewear shall be supplied.Laser safety classification: The complete system and each applicable laser source/probe shall comply with the applicable laser safety classification and standards. If Class 3B laser is offered, appropriate safety controls and protective eyewear shall be supplied.
16Electrical safety: Suitable for operation on 230 V AC, 50 Hz Indian mains supply, with appropriate protection. Input range may be universal (e.g. 100–240 V AC, 50/60 Hz) or equivalent.Electrical safety: Suitable for operation on 230 V AC, 50 Hz Indian mains supply, with appropriate protection. Input range may be universal (e.g. 100–240 V AC, 50/60 Hz) or equivalent.
17Construction: Compact, robust and easy-to-clean medical-grade housing suitable for hospital use.Construction: Compact, robust and easy-to-clean medical-grade housing suitable for hospital use.
18Portability: Bench-top/portable configuration preferred, with provision for safe handling and storage of probes/accessories.Portability: Bench-top/portable configuration preferred, with provision for safe handling and storage of probes/accessories.
19Cooling: Adequate thermal management/cooling system to ensure safe and stable operation during specified duty cycle.Cooling: Adequate thermal management/cooling system to ensure safe and stable operation during specified duty cycle.
20Minimum required number of therapeutic laser probes/applicators as per offered configuration.Minimum required number of therapeutic laser probes/applicators as per offered configuration.
21Protective laser safety eyewear appropriate to the wavelength(s) and laser safety class supplied; adequate quantity for operator and patient.Protective laser safety eyewear appropriate to the wavelength(s) and laser safety class supplied; adequate quantity for operator and patient.
22Probe/applicator holder or stand, where applicable.Probe/applicator holder or stand, where applicable.
23Power cable and all necessary connection cables.Power cable and all necessary connection cables.
24Calibration/test facility or accessories required for routine performance verification, where applicable.Calibration/test facility or accessories required for routine performance verification, where applicable.
25User/operator manual and service/maintenance manual in English.User/operator manual and service/maintenance manual in English.
26Any other accessories necessary for safe and complete operation of the quoted system.Any other accessories necessary for safe and complete operation of the quoted system.
27The offered equipment shall comply with applicable Indian statutory requirements and applicable international standards for medical electrical equipment and laser safety.The offered equipment shall comply with applicable Indian statutory requirements and applicable international standards for medical electrical equipment and laser safety.
28The bidder shall provide valid conformity/safety certificates applicable to the quoted model, as required under prevailing Indian regulations and procurement conditions.The bidder shall provide valid conformity/safety certificates applicable to the quoted model, as required under prevailing Indian regulations and procurement conditions.
29Laser safety eyewear shall be supplied according to the wavelength(s) of the offered laser system and shall carry appropriate identification/marking.Laser safety eyewear shall be supplied according to the wavelength(s) of the offered laser system and shall carry appropriate identification/marking.
30The bidder shall clearly state the laser classification, wavelength(s), maximum output power and relevant safety standard(s) in the technical offer.The bidder shall clearly state the laser classification, wavelength(s), maximum output power and relevant safety standard(s) in the technical offer.
31Where applicable, the equipment shall comply with IEC 60825-1 or the latest applicable edition/standard, along with applicable medical electrical safety requirements.Where applicable, the equipment shall comply with IEC 60825-1 or the latest applicable edition/standard, along with applicable medical electrical safety requirements.
32All electrical accessories supplied with the system shall be suitable for Indian mains supply and hospital use.All electrical accessories supplied with the system shall be suitable for Indian mains supply and hospital use.
33Quoted model should comply with CE/US FDA, ISO 13485 & IEC 60601-2-22 Certificate.Quoted model should comply with CE/US FDA, ISO 13485 & IEC 60601-2-22 Certificate.

AI Tender Summary

OUR REF NO 57356680
AUTHORITY Boards / Undertakings / PSU
TENDER VALUE Ref. Documents
LAST DATE 25-09-2026
Authority
Authority Name Tata Memorial Centre
Work Description Bids Are invited for Low Level Laser Therapy Machine - System Type: Computerized Low-Level Therapeutic Laser / Photobiomodulation System With Programmable Treatment Parameters. , Laser Source: Semiconductor Therapeutic Laser Source(S), Such As Gaalas Or Equivalent Technology, Suitable For Lllt/Photobiomodulation. , Operating Mode: Continuous And Pulsed Modes Shall Be Available. , Wavelength: At Least One Therapeutic Wavelength In The Red/Near-Infrared Range; System Shall Support Clinically Appropriate Wavelengths. Multiple Interchangeable Probes/Applicators May Be Offered. , Output Power: Variable/Programmable Therapeutic Output Power With Suitable Control Through The System Interface. The Offered Configuration Shall Provide Adequate Output For Intended Clinical Applications. , Pulse Frequency: Programmable Pulse Frequency Covering A Clinically Useful Range, Preferably Extending From Low-Frequency Operation To At Least Several Khz, As Applicable To The Offered System. , Treatment Time: Programmable Treatment Timer With A Minimum Range Of 0–60 Minutes Or Wider. , Treatment Parameter Control: User-Selectable Control Of Relevant Treatment Parameters Such As Wavelength/Probe, Output Power, Mode, Pulse Frequency And Treatment Time, As Applicable. , Display / User Interface: Colour Touchscreen Or Equivalent User-Friendly Display For Setting, Monitoring And Confirming Treatment Parameters. , Probe/Applicator Detection: Automatic Recognition/Detection Of Connected Therapeutic Probe(S)/Applicator(S) Is Preferred. , Treatment Indication / Preset: Programmable Or Preconfigured Treatment Protocols/Presets For Commonly Used Clinical Applications, With Facility For User-Defined Settings. , Memory: Patient/Treatment Parameter Storage Or User Memory Facility Is Preferred, With Access Control As Applicable. , Safety Features: Audible/Visual Indication Of Treatment Status And/Or Completion, Controlled Activation, Fault Indication, Emergency Stop Or Equivalent Safety Provision, And Protection Against Unintended Laser Emission. , Password/Access Control: User Access Control/Password Protection For Treatment Settings And Stored Data, Where Applicable. , Laser Safety Classification: The Complete System And Each Applicable Laser Source/Probe Shall Comply With The Applicable Laser Safety Classification And Standards. If Class 3B Laser Is Offered, Appropriate Safety Controls And Protective Eyewear Shall Be Supplied. , Electrical Safety: Suitable For Operation On 230 V Ac, 50 Hz Indian Mains Supply, With Appropriate Protection. Input Range May Be Universal (E.G. 100–240 V Ac, 50/60 Hz) Or Equivalent. , Construction: Compact, Robust And Easy-To-Clean Medical-Grade Housing Suitable For Hospital Use. , Portability: Bench-Top/Portable Configuration Preferred, With Provision For Safe Handling And Storage Of Probes/Accessories. , Cooling: Adequate Thermal Management/Cooling System To Ensure Safe And Stable Operation During Specified Duty Cycle. , Minimum Required Number Of Therapeutic Laser Probes/Applicators As Per Offered Configuration. , Protective Laser Safety Eyewear Appropriate To The Wavelength(S) And Laser Safety Class Supplied; Adequate Quantity For Operator And Patient. , Probe/Applicator Holder Or Stand, Where Applicable. , Power Cable And All Necessary Connection Cables. , Calibration/Test Facility Or Accessories Required For Routine Performance Verification, Where Applicable. , User/Operator Manual And Service/Maintenance Manual In English. , Any Other Accessories Necessary For Safe And Complete Operation Of The Quoted System. , The Offered Equipment Shall Comply With Applicable Indian Statutory Requirements And Applicable International Standards For Medical Electrical Equipment And Laser Safety. , The Bidder Shall Provide Valid Conformity/Safety Certificates Applicable To The Quoted Model, As Required Under Prevailing Indian Regulations And Procurement Conditions. , Laser Safety Eyewear Shall Be Supplied According To The Wavelength(S) Of The Offered Laser System And Shall Carry Appropriate Identification/Marking. , The Bidder Shall Clearly State The Laser Classification, Wavelength(S), Maximum Output Power And Relevant Safety Standard(S) In The Technical Offer. , Where Applicable, The Equipment Shall Comply With Iec 60825-1 Or The Latest Applicable Edition/Standard, Along With Applicable Medical Electrical Safety Requirements. , All Electrical Accessories Supplied With The System Shall Be Suitable For Indian Mains Supply And Hospital Use. , Quoted Model Should Comply With Ce/Us Fda, Iso 13485 & Iec 60601-2-22 Certificate.
Basic Detail
Tender No GEM/2026/B/7994940
Bidding Type Tender
Location
City Muzaffarpur
State Bihar
Key Dates
Publish Date 04 Sep 2026
Submission Date 25 Sep 2026
Open Date 26 Sep 2026
Finance
Tender Value Ref. Documents
Tender Fee Ref. Documents
EMD 1.10 Lakhs
Exemption Available
Document List
cf484af5-0eeb-4574-ab51-1d167f0da904.pdf
laser_therapy_system_technical_specification_2026-09-03-15-54-13_3059ce7dd5f3f5fce2d25b859c689f14.xlsx
laser_therapy_system_2026-09-03-15-54-13_21dd35b9e7bc061b4879ee320f82ae11.pdf

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Tender Timeline

Sep 04, 2026
11:30 IST

Tender Published

Tender notice published.

Completed
Sep 25, 2026
17:00 IST

Bid Submission Deadline

Online submission via eProcurement portal.

Upcoming · 18 days
Sep 26, 2026

Bid Opening Date

Technical bids will be opened and evaluated.

Upcoming · 19 days

Tender Documents

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pdf

cf484af5-0eeb-4574-ab51-1d167f0da904.pdf

xlsx

laser_therapy_system_technical_specification_2026-09-03-15-54-13_3059ce7dd5f3f5fce2d25b859c689f14.xlsx

pdf

laser_therapy_system_2026-09-03-15-54-13_21dd35b9e7bc061b4879ee320f82ae11.pdf

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