| Product Standard Compliance | The capacitor design should comply with the applicable international standard for low-voltage AC power capacitors. | Test reports, technical datasheets, rated-voltage and frequency specifications, and standard references. | IEC 60831-1 for general requirements and IEC 60831-2 for destructive testing, where applicable. | 20% | — |
| Quality Management System | A documented and independently audited quality system should control production, inspection, corrective action, and traceability. | Current ISO 9001 certificate, certification scope, issuing body, audit status, and certificate validity. | ISO 9001 certification covering the relevant capacitor manufacturing site and product scope. | 15% | — |
| Environmental and Chemical Compliance | Materials and production controls should address restricted substances and environmental management requirements. | RoHS and REACH declarations, material declarations, supplier compliance records, and environmental certificates. | Current RoHS/REACH documentation; ISO 14001 is an additional indicator of environmental management. | 10% | — |
| Electrical Performance | Capacitance, capacitance tolerance, loss angle, insulation performance, and discharge behavior should remain within specification. | Routine test records, sample test reports, calibrated measurement equipment, and product inspection plans. | Typical project specifications should define capacitance tolerance, dielectric loss, insulation resistance, and discharge requirements before ordering. | 15% | — |
| Safety and Protection Design | The construction should include appropriate internal protection and safe failure behavior for the intended application. | Construction drawings, overpressure disconnector details, self-healing film information, safety test reports, and application limitations. | Confirm self-healing technology, overpressure protection, discharge provisions, and suitability for the specified voltage and temperature. | 15% | — |
| Manufacturing Capability | The facility should have controlled processes for film metallization, winding, assembly, impregnation or filling, sealing, and final testing. | Factory audit, process flow chart, equipment list, maintenance records, production capacity, and in-process inspection records. | Documented process controls, batch traceability, calibrated equipment, and capacity aligned with the required annual volume. | 10% | — |
| Testing Laboratory | Testing should be performed with calibrated instruments and, where necessary, verified by an independent laboratory. | Calibration certificates, laboratory procedures, test equipment inventory, and third-party laboratory reports. | Calibration traceable to recognized national or international standards; independent testing preferably performed by an ISO/IEC 17025-accredited laboratory. | 5% | — |
| Reliability and Life Expectancy | Expected service life should be evaluated against operating temperature, voltage stress, switching frequency, harmonics, and installation conditions. | Life-test data, temperature-category information, derating curves, warranty terms, and field-failure analysis procedure. | Supplier provides application-specific life data and clearly states limits for temperature, overvoltage, overcurrent, and harmonic distortion. | 5% | — |
| Documentation and Traceability | Each production batch should be traceable to raw materials, manufacturing records, inspection results, and shipment documents. | Batch codes, certificates of conformity, inspection reports, packing lists, and retention-period policy for quality records. | Full batch traceability from incoming materials through final shipment, with records available for customer review. | 3% | — |
| Commercial and Service Support | The supplier should provide stable lead times, technical support, warranty handling, and corrective-action communication. | Quotation validity, lead-time commitment, warranty policy, response-time agreement, nonconformity procedure, and sample approval process. | Written specifications, pre-production samples, defined acceptance criteria, and documented corrective-action response. | 2% | — |