Contrast Media Injector
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This page explains how Syringe Assembly is classified within Machinery and Equipment Manufacturing. Technical values and manufacturer relationships are research references; confirm the current specification and supplier evidence for each order.
A precision medical device component that holds and dispenses contrast media during medical imaging procedures.
Technical details and manufacturing context for Syringe Assembly
| Parameter | Typical range | Notes & selection driver |
|---|---|---|
| Nominal Volume | 10–200 mL | Common sizes for contrast media deliveryISO 7886-1 |
| Luer Lock Connection | 6% taper | Ensures secure attachment to catheterISO 594-1 |
| Plunger Force | 15–40 N | Required to maintain steady flowISO 7886-1 |
| Leakage Rate | ≤0.1 mL/min | At 300 kPa internal pressureISO 7886-1 |
| Temperature Range | 5–40 °C | Storage and operation |
| Material | PC, PP, silicone | Biocompatible gradesISO 10993-1 |
| Sterilization Method | EO, gamma | Must not degrade materialISO 11135 |
| Weight | 20–80 g | Depends on volume and material |
| Tolerance on Dimensions | ±0.1 mm | Critical for sealing and fitISO 2768-m |
Ranges are indicative industry figures for RFQ preparation, not a supplier commitment. Confirm every value and standard with the legal manufacturer before ordering.
Commonly used trade names and technical identifiers for Syringe Assembly.
This component is essential for the following industrial systems and equipment:
| pressure: | Up to 150 psi (10.3 bar) maximum working pressure |
| flow rate: | 0.1 to 10 mL/sec typical, depending on syringe size and application |
| temperature: | 15°C to 40°C (operating), -20°C to 50°C (storage) |
| slurry concentration: | Not applicable - designed for homogeneous contrast media solutions only |
Indicative industry ranges for design and RFQ preparation. Confirm the exact figures and applicable standard with the manufacturer before specifying.
Quoted from the published standard.
2 companies list this product among what they make. Company figures are quoted from each company's own website; every card states where the relationship came from.
Manufacturer listings support early research and capability understanding. They are not certification, ranking, or transaction guarantees.
A practical evidence checklist for RFQ preparation and supplier evaluation.
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The nominal volume ranges from 10 to 200 mL, as listed in the directory. However, the exact volume for a specific model must be confirmed with the legal manufacturer or supplier.
The directory lists ISO 7886-1 for volume, plunger force, and leakage rate; ISO 594-1 for the Luer lock connection; ISO 10993-1 for biocompatibility; and ISO 11135 for sterilization methods. These are reference standards for verification, not proof of certification.
The materials on file include medical-grade polycarbonate, stainless steel, and silicone rubber. These are typical materials, but the exact grades and suitability must be verified with the manufacturer.
The directory indicates that ethylene oxide (EO) and gamma irradiation are acceptable sterilization methods, as per ISO 11135. However, the specific sterilization method must be validated for the actual product.
Editorial classification, named public sources where available, and source-reviewed manufacturer records.
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