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LAPAROSCOPIC EQUIPMENT | MUMBAI, INDIA

CO2 Insufflator for Laparoscopic Surgery

Bharat Surgical Co. accepts enquiries for selected CO2 insufflators used as part of compatible laparoscopic equipment systems. Established in 1975 and based in Mumbai, India, the company supports hospitals, surgeons, biomedical teams, dealers, distributors, institutional buyers and export enquiries subject to exact model, intended use, technical specification, documentation and service confirmation.

For an accurate quotation, share the required maximum flow and pressure range, gas source and inlet connection, preferred display and alarm functions, compatible tubing and filter set, existing insufflator details, mains supply, quantity, destination, installation, training, inspection, regulatory and after-sales requirements. Bharat Surgical will confirm the proposed model, accepted specification, supplied accessories, evidence, price and delivery in writing.

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Established 1975
Mumbai Manufacturer & Supplier
B2B & Export Enquiries
Specification-Led Selection
CO2 Insufflator for Laparoscopic Surgery
Overview

What Is a CO2 Insufflator?

A CO2 insufflator is medical electrical equipment designed to deliver carbon dioxide through a compatible insufflation circuit while monitoring and controlling system parameters defined by the exact model. It forms one part of a laparoscopic equipment setup and must be selected together with its approved gas source, inlet components, outlet connector, tubing, filters, access instruments, installation conditions and instructions for use.

Maximum flow, selectable pressure, actual delivered performance, alarm behavior and recovery characteristics are not interchangeable terms. A higher headline flow rate does not by itself establish suitability, performance or safety. Buyers should compare the complete model specification, evidence, accessories, controls and lifecycle support rather than ordering from a flow-rate label alone.

Specifications Guide

CO2 Insufflator Specification Framework

Use this framework to compare models and ensure correct technical approvals.

System Element Information to Confirm
Equipment Identity Legal manufacturer, brand, exact model and revision, intended use, supplied condition, country of origin, serial-number format and current active status.
Flow Specification Maximum selectable or rated flow, available steps or control method, measurement basis, tolerance and any model-defined operating limitations.
Pressure Specification Selectable range, displayed parameter, control accuracy, measurement basis, alarm thresholds, over-pressure response and limitations stated in the product evidence.
Gas Supply CO2 source, cylinder or central pipeline compatibility, inlet pressure range, regulator requirements, hose, inlet connector, filtration and gas-quality responsibilities.
Patient Circuit Outlet connector, approved tubing set, filters, stopcocks or adapters, reusable/disposable/sterile status, quantities, replacement interval and traceable part numbers.
Display and Controls Display type, pressure/flow/gas-use information, set controls, presets or memory, language, indicators, start/stop and reset behavior supported by exact documentation.
Alarms & Protective Functions Audible/visual alarms, occlusion or no-flow indication, low-gas warning, over-pressure response, self-test, error codes and power-interruption behavior.
Optional Functions Gas warming, smoke management, flow sensing, data output, remote control or other functions only when supported by the proposed model and approved accessories.
Electrical and Physical Mains voltage/frequency, power input, electrical class, applied-part classification, ingress protection where applicable, dimensions, weight, mounting and environmental limits.
Evidence and Documents Applicable safety/EMC and endoscopic-equipment standards with editions, test reports or certificates, registration, labels, IFU, service information and traceability.
Lifecycle Support Installation, acceptance testing, user/biomedical training, preventive maintenance, performance verification or calibration status, spares, software, warranty, AMC and service response.
RFQ Guidelines

CO2 Insufflator RFQ Checklist

Submit one technical line for each required configuration to prevent processing gaps.

RFQ Field Information to Provide
Requirement New installation, replacement, upgrade, additional theatre, standardization, tender, rate contract, dealer stock or export project.
Department and Scope Laparoscopy, gynecology, urology or other approved intended scope; state the facility requirement without requesting clinical settings.
Performance Required maximum flow, pressure range, display and measurement requirements, tolerances and any prohibited or mandatory functions.
Gas Source Cylinder or central supply, available inlet pressure, regulator, hose, connector, gas-standard/site requirements and existing infrastructure.
Circuit and Accessories Outlet connector, tubing, filters, adapters, stopcocks, warming set or other approved accessories, part numbers, status and quantities.
Alarms and Controls Required pressure, flow, occlusion, low-gas, system-error and power indications; control, display, language and self-test requirements.
Electrical and Installation Site voltage/frequency, plug, earthing, UPS policy, trolley/shelf, room conditions, installation and acceptance-testing requirements.
Existing Equipment Make/model/serial, nameplate and connector photographs, gas hose, regulator, outlet, circuit, service history and reason for replacement.
Documents Datasheet, IFU, labels, standards declaration, test evidence, registration, current ISO, origin, inspection, performance, warranty, tender and export documents.
Training and Service User and biomedical training, preventive-maintenance schedule, service coverage, spares, software, AMC, response expectations and escalation route.
Commercial and Logistics Quantity, destination, required date, demo policy, MOQ, price, taxes, freight, payment, credit, packing, insurance, commissioning and quotation validity.

Clinical and Safety Boundary

This page supports equipment identification and procurement. It is not a clinical operating guide, a substitute for the manufacturer's instructions, or authorization to select pressure, flow, access technique, tubing, filters or procedure settings. Selection, installation, testing, use, cleaning, maintenance and release into service must be controlled by qualified healthcare and biomedical personnel under the applicable product information, hospital procedures and regulatory requirements.

Category Boundary Notice

Keep this page limited to CO2 insufflator equipment and the exact quoted insufflation set. Route Veress needles, trocars and compatible hand instruments to Laparoscopic Instruments; scopes and camera-system components to Endoscopes & Accessories; illumination to LED Light Source; and training equipment to Endo Trainer. Do not merge anaesthesia gas equipment, medical-gas pipeline systems, smoke evacuators, unrelated pumps or generic air compressors into this category.

Safety, Standards & Documentation

IEC 60601-2-18 establishes particular basic-safety and essential-performance requirements for endoscopic equipment and supplements IEC 60601-1. The quotation should state the actual standards, editions, amendments, reports and certificates applicable to the proposed unit. Gas source, regulator, inlet hose, outlet connector, tubing and filters should be inspected and used only in approved combinations.

Receiving, Installation & Lifecycle Control

On receipt, qualified personnel should verify the cabinet serials, gas inlets, outlets, regulators, hoses, certificates, and physical condition. Installation, gas connection, electrical safety, functional testing, pressure/flow calibration, and clinical release must follow manufacturer guides. The website does not publish a single generic maintenance cycle; plans are model-specific.

Audience Routes

Support for Different Buyers

We coordinate specifications across distinct B2B buyer workflows.

Hospitals & Surgery Centres

Hospitals may submit single-unit, replacement, multi-OT, BOQ, tender, rate-contract or standardization requirements. Include performance, gas infrastructure, patient circuits, acceptance tests, training, documents, warranty, maintenance, spares and service expectations.

  • Action: Submit BOQ / tender schedule
  • Infrastructure: Cylinder or pipeline verification
  • SLA: Defined service coverage and spares

Biomedical & Procurement Teams

Biomedical and procurement teams should control the purchase through an approved technical comparison. Ask for model-level datasheets, applicable standards and editions, gas and electrical interfaces, accessories, maintenance, performance-verification terms, spares and warranty rather than accepting an unqualified equivalent.

  • Interface: Gas hose standards and electrical class
  • Evidence: Compliance certificate verification
  • Responsibility: Final site acceptance & release

Surgeons & Clinical Users

Clinical users can state the approved departmental scope, preferred workflow and equipment features needed for technical evaluation. Flow, pressure, access method and clinical use remain subject to the healthcare organization's governance, product instructions and qualified review.

  • Scope: Laparoscopy, gynecology, or urology needs
  • Workflow: Display readability and alarm indicators
  • Governance: Institutional clinical selection protocols

Dealers & Distributors

Submit the target market, buyer segment, forecast quantity, technical specification, circuit demand, registration, tender, demo, training, warranty and service expectations. A purchase does not grant distribution rights without written terms.

  • Demand: Local catalog requirements & forecasts
  • Role: Site delivery, commissioning, and training
  • Terms: Standardized dealer and distributor agreements

International & Project Suppliers

Provide the destination country, importer or project details, mains and plug, gas source and connector, approved specification, quantity, circuits, labelling, language, registration, shipping, installation, training, warranty and local service responsibilities.

  • Inlet: Country-specific pipeline plug standards
  • Power: Voltage, frequency and wall sockets
  • Compliance: Regulatory certificate confirmation

Tender & Lifecycle Support

For multi-unit tenders. Provide detailed spec sheets, delivery milestones, and training plans. Selected equipment models may be assessed for preventive maintenance plans, AMC options, and spares availability.

  • Tenders: Permissible deviations and milestones
  • Demo: Technical evaluation trials on-site
  • Maintenance: Spares, software support and AMC contracts
CO2 Insufflator FAQs

Frequently Asked Questions

Common queries regarding our laparoscopic insufflation equipment and technical verification.

It is medical electrical equipment designed to deliver carbon dioxide through an approved circuit while monitoring and controlling model-defined system parameters. The complete setup includes the gas source, inlet components, outlet connection, tubing, filters, access equipment and instructions.

Bharat Surgical accepts enquiries for selected CO2 insufflators. Because current public catalogue records are incomplete and inconsistent, the active model, specification, documents, supplied set and service terms must be confirmed before ordering.

No. Compare intended use, pressure control, alarms, gas input, circuit compatibility, evidence, installation, maintenance and service. A larger L/min figure alone does not establish suitability or superior performance.

Central-supply compatibility is model- and site-specific. Provide the available gas standard, outlet, pressure and connector, then obtain written confirmation of the approved hose, regulator or interface and installation responsibility.

Only if the written quotation lists them. Confirm outlet connector, tubing set, filter, adapters, quantities, part numbers, supplied condition and whether each item is reusable or single-use.

Do not assume it. Ask whether the exact model has an approved warming function, which accessories it requires, what is included and which evidence and instructions apply.

Do not infer smoke management from the term insufflator. Confirm whether the exact model has any approved smoke-related function, required tubing or filters and limitations; otherwise treat smoke evacuation as separate equipment.

IEC 60601-2-18 covers particular safety and essential-performance requirements for endoscopic equipment and supplements IEC 60601-1. Other electrical, EMC, risk-management or jurisdictional requirements may apply. Verify the exact standards and editions for the proposed model.

Selected units may be assessed, but repairability depends on brand, model, serial number, fault, parts, software and authorized support. Charges, approval, turnaround, tests, warranty and shipping must be confirmed after inspection.

Send Your CO2 Insufflator Specification

Share the required department scope, maximum flow, pressure range, gas source, inlet regulator/hose/connector, outlet tubing and filters, display and alarms, optional functions, mains supply, quantity, destination, required date, installation, training, inspection, regulatory, warranty and service needs. Attach a BOQ, tender schedule, previous equipment nameplate or connector photographs for a faster technical and commercial response.

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Laparoscopic Instruments • Laparoscopic Trocar • Veress Needle • Endoscopes & Accessories • Endo Trainer • Bulk Order / B2B Enquiry • Quality Standards & Certifications • Repair & Service Backup