AGM-30

Overview

The Ohmite AGM-30 is a single-phase, single-stage power line EMI filter designed for medical applications. It operates at 250 VAC with a 30 A current rating and supports 50/60 Hz frequencies. The unit features chassis mounting via tab connectors and exhibits a leakage current of 340 uA. Dimensions are 100 mm length, 86 mm width, and 40 mm height, weighing approximately 500 g. It complies with UL, CSA, and IEC/EN standards.

Feature Summary

• Designed specifically for medical equipment requiring high performance and minimal leakage currents.
• Complies with the IEC 60601-1 standard for medical electrical equipment safety.
• Utilizes a single-stage filtering architecture to suppress electromagnetic interference.

Applications

• Diagnostic equipment
• Surgical beds
• X-ray machines

Procurement Notes

Verify component status carefully as the AGM-30 is listed as obsolete or end-of-life by major distributors. Confirm availability through authorized channels or secondary markets if sourcing is required. Ensure that any replacement components meet the same medical compliance standards, specifically IEC 60601-1, to maintain system certification integrity.

Selection Notes

Select this component only when medical-grade isolation and low leakage current are mandatory requirements. The 30 A rating suits high-power medical devices. Verify that the chassis mount form factor and tab connector termination align with the target enclosure design. Consider the physical dimensions and weight constraints during mechanical integration planning.

Part Context

The AGM-30 belongs to the AGM Series from Ohmite, which specializes in filters for medical applications. This series is engineered to meet strict regulatory standards for patient safety. The manufacturer, Ohmite, is known for power resistors and related power conditioning components, leveraging expertise in high-energy handling and thermal management.

Replacement Considerations

Publicly confirmed substitute part numbers are not available in the provided documentation. Due to the obsolete lifecycle status and specific medical compliance requirements (IEC 60601-1), direct replacements must be verified against original datasheet specifications for leakage current and insulation properties.