Source ISO9809 3 Medical Oxygen Cylinder for Hospitals, Clinics, and Home Care
Find 30 verified listings for the ISO9809 3 medical oxygen cylinder to compare specifications like water capacity, working pressure, and material. Buyers can evaluate options from manufacturers in China for hospital, clinic, and home care applications.
Key considerations
Products List
Comprehensive Sourcing Guide
Strategic Sourcing Guide for ISO 9809 Compliant Medical Oxygen Cylinders
Understanding the Technical Profile of ISO 9809 Cylinders
When sourcing medical oxygen cylinders, the primary technical anchor is the Executive Standard En ISO9809-1, which governs the design, manufacture, and testing of seamless steel gas cylinders. This standard ensures that the vessel can safely contain gases under high pressure, a critical requirement for medical applications where purity and structural integrity are non-negotiable. The observed product data indicates that cylinders meeting this standard often feature specific dimensions and capacities. For instance, a typical model designated as 267-40L-150Bar suggests a water capacity of 40 liters with an outer diameter of 267 millimeters. Another variant, the 232-47L-200Bar, demonstrates a water capacity of 47 liters and an outer diameter of 232 millimeters. These physical attributes are not merely descriptive; they dictate the storage volume and the spatial requirements for hospital logistics and transport.
The pressure level is another defining technical characteristic. Medical oxygen cylinders generally fall within the high-pressure category, defined as operating between 10.0 MPa and 100.0 MPa. Specific data points highlight working pressures of 200 bar and even higher test pressures reaching 300 bar, indicating a robust safety margin over the standard working pressure. The material composition is equally vital; the supply chain data references materials such as 34CrMo and 37mn, which are alloy steels selected for their high tensile strength and resistance to fatigue under cyclic loading. The weight of these vessels, measured without the valve or cap, ranges from 47 kg to 52.5 kg, depending on the capacity and wall thickness required to withstand the internal pressure. Understanding these specifications allows procurement teams to calculate shipping costs, storage rack load limits, and handling requirements accurately before placing an order.
Compliance Verification and Certification Protocols
Compliance with international standards is the first line of defense in ensuring patient safety and regulatory adherence. The En ISO9809-1 standard is the benchmark for these vessels, but buyers must also verify the presence of specific certifications such as CE and ISO. These marks indicate that the manufacturing process has undergone rigorous third-party auditing to ensure consistency and safety. However, the presence of a certification mark on a product listing does not automatically guarantee that every unit in a shipment is certified; it is a verification of the production line's capability. Buyers must explicitly request the Certificate of Conformity (CoC) for the specific batch they are purchasing.
The distinction between the executive standard and the product standard is crucial. While En ISO9809-1 provides the overarching framework, the product standard may reference specific manufacturing tolerances, such as the outer diameter of 267mm or 232mm. Procurement officers should verify that the supplier's documentation explicitly cites the correct version of the standard. Furthermore, the material specifications, such as the 34CrMo alloy, must be cross-referenced with the test pressure requirements. The data indicates a hydraulic test pressure of 300 bar against a working pressure of 200 bar, a ratio that must be maintained to ensure the cylinder does not fail under stress. Buyers should not rely on general claims of compliance but must demand test reports that validate the specific pressure ratings and material properties for the ordered model.
Cost Drivers and Pricing Variables in the Market
The pricing for medical oxygen cylinders is influenced by a complex interplay of material costs, manufacturing complexity, and order volume. The observed price range in the market spans from 1.8 USD to 100,000 USD, a vast disparity that reflects the difference between individual components, small-scale custom units, and large industrial batches. For standard medical cylinders, the cost is heavily driven by the raw material price of steel alloys like 34CrMo and 37mn, which fluctuates with global commodity markets. Additionally, the customization level significantly impacts the final price. Products listed with "Customization: Available" or "Customized" options often carry a premium due to the additional engineering and tooling required.
Minimum Order Quantity (MOQ) is another critical cost driver. The data shows an MOQ range from 1 to 1000 units, with specific listings indicating an MOQ of 500 pieces for certain configurations. Ordering below the standard MOQ often results in higher per-unit costs due to the inefficiencies of small-batch production. Conversely, larger orders may benefit from economies of scale but require significant upfront capital and storage capacity. The packaging method, described as "Based on Customer's Request" or "Carton/Pallet," also adds to the cost. Custom packaging solutions designed to prevent damage during transit or to meet specific hospital inventory protocols will increase the unit price. Buyers must balance the need for customization against the budget constraints, ensuring that the chosen configuration does not introduce unnecessary expenses that could be avoided with standard specifications.
Typical Applications and Functional Requirements
Medical oxygen cylinders serve multiple functions beyond simple gas storage, including reaction, heat pressure, separation, and storage of pressure vessels. The primary application is the delivery of medical-grade oxygen to patients in hospitals, clinics, and home care settings. The "Gas" application tag confirms their suitability for this purpose, but the specific design must support the purity requirements of medical use. The cylinders are designed to be "New" condition, ensuring no prior contamination or structural fatigue. The "Closed" structure and "Spring" mechanism in related components suggest a design focused on maintaining a sealed environment to prevent moisture ingress, which is critical for medical oxygen purity.
The connection type is typically a thread, with specific standards like En15202/G12 for the outlet thread and a 25e inlet thread. These standardized connections ensure compatibility with medical regulators and flow meters used in clinical settings. The "Low Temperature" attribute indicates that these cylinders are designed to withstand the thermal stresses associated with rapid gas expansion, which can cause significant cooling. This is particularly important in high-flow medical scenarios. The ability to store gas, liquid, and solid objects (as noted in storage objects) suggests a versatility that, while primarily focused on gas, requires the vessel to maintain integrity under various physical states. Buyers must ensure that the selected cylinder's functional attributes align with the specific medical protocols of their facility, particularly regarding flow rates and temperature management.
Supplier Evaluation and Origin Considerations
Evaluating a supplier for medical oxygen cylinders requires a deep dive into their operational capabilities and geographic origin. The data points to "Anhui China" and general "China" origins as key sourcing locations. While these regions are major manufacturing hubs, buyers must verify the specific factory's track record in producing medical-grade equipment. The presence of "Customization: Available" and "Customized" attributes suggests that the supplier has the flexibility to adapt to specific client needs, a valuable trait for large healthcare networks with unique requirements. However, the ability to customize does not imply a lack of standardization; the core product must still adhere to the En ISO9809-1 standard.
Supplier reliability is further assessed through their quality control processes and certification status. A supplier claiming CE and ISO certifications must be able to provide valid, up-to-date documentation. The "Condition: New" attribute implies a focus on fresh production, but buyers should also inquire about the supplier's inventory management to ensure that the cylinders are not stored in conditions that could degrade the metal or seals over time. The "Water Capacity" and "Weight" specifications serve as verification points; a supplier claiming a 40L capacity but delivering a cylinder weighing significantly less than the 47kg baseline may be compromising on wall thickness or material quality. Buyers should conduct on-site audits or request third-party inspection reports to validate these physical attributes before committing to a large order.
Quality Control and Long-Term Procurement Strategy
Implementing a robust quality control (QC) strategy is essential for the long-term success of medical oxygen cylinder procurement. The QC process should begin with the verification of the "Executive Standard: En ISO9809-1" and the "Standard: Standard" compliance. Buyers must ensure that the hydraulic test pressure of 300 bar is consistently applied during the manufacturing process, as this is a critical safety threshold. The "Working Pressure" of 200 bar must be clearly marked on the cylinder, and the "Pressure Level" must be confirmed as High Pressure (10.0MPa≤p<100.0MPa). Regular non-destructive testing, such as ultrasonic or magnetic particle inspection, should be mandated to detect any micro-cracks or material defects that could lead to catastrophic failure.
Long-term procurement considerations involve establishing a partnership with a supplier that can provide consistent quality over time. The "Product Packing" being "Based on Customer's Request" offers an opportunity to standardize packaging for efficient logistics and inventory management. Buyers should negotiate terms that include regular quality audits and the right to reject batches that do not meet the specified weight, dimensions, or pressure ratings. The "Material" specification of 34CrMo or 37mn must be verified through mill test certificates for every batch. By maintaining strict adherence to these technical and procedural standards, healthcare organizations can ensure a reliable supply of safe, high-quality medical oxygen cylinders, minimizing the risk of equipment failure and ensuring patient safety.
FAQs
What executive standard governs these medical oxygen cylinders?
The cylinders comply with the En ISO9809-1 executive standard for seamless steel gas cylinders. This standard ensures structural integrity and safety for high-pressure medical gas storage applications.
Which certifications are required for these pressure vessels?
Valid certifications include CE and ISO marks indicating third-party auditing of the manufacturing process. Buyers must request specific batch Certificates of Conformity to verify compliance.
How is the working pressure defined for these high-pressure cylinders?
These vessels operate at a working pressure of 200 bar with a hydraulic test pressure of 300 bar. This ratio ensures a robust safety margin for medical oxygen delivery.
Can I find cylinders with a 40-liter water capacity?
Yes, models like 267-40L-150Bar feature a 40-liter water capacity and an outer diameter of 267mm. These dimensions dictate storage volume and spatial requirements for hospital logistics.
What material is used to construct these high-pressure vessels?
The cylinders are constructed from alloy steels such as 34CrMo or 37mn for high tensile strength. These materials resist fatigue under cyclic loading required for medical applications.
What is the minimum order quantity for these customized cylinders?
The minimum order quantity is 500 pieces for certain configurations. Ordering below this threshold may result in higher per-unit costs due to small-batch production inefficiencies.
Where are these medical oxygen cylinders manufactured?
The products originate from manufacturing hubs in Anhui, China. Buyers should verify the specific factory track record for producing medical-grade equipment to ensure quality.





























