| S1 | ISO 12100:2010 Safety of Machinery | Official ISO standard record | Establishes risk assessment and reduction rules for customized mechanical integrations. | Official record Official page confirms status and scope; licensed standard text must be checked for clause-level obligations. | 2026-07-28 |
| S2 | IEC 60034-1:2026 Rotating Electrical Machines | Official IEC publication record | Defines rating and performance terminology used when planning custom motor winding validation. | Official record Use as a motor-rating baseline only; actuator assemblies may require additional application standards. | 2026-07-28 |
| S3 | ISO 13485:2016 Medical Devices Quality Management | Official ISO standard record | Mandates product design traceability and verification checklists for surgical joints. | Official record QMS alignment does not certify a final surgical robot; customer regulatory files and jurisdiction rules still apply. | 2026-07-28 |
| S4 | ISO 10218-1:2025 Industrial Robots - Safety Requirements | Official ISO standard record | Frames industrial robot safety requirements that influence safe states, braking logic, and control boundaries. | Official record Collaborative robot applications may also require ISO/TS 15066 and application-level risk assessment. | 2026-07-28 |
| S5 | IEC 60601-1-2 Medical Electrical Equipment EMC | Official IEC publication records | Provides EMC baselines for actuator electronics used inside medical electrical equipment or systems. | Official record Final test plans must name the exact collateral-standard edition and intended electromagnetic environment. | 2026-07-28 |
| S6 | ISO 13849-1:2023 Safety-Related Parts of Control Systems | Official ISO standard record | Specifies Performance Level (PL) and category targets for safety brake and STO circuits. | Official record Does not define the required PLr for a given machine; PLr must come from the robot risk assessment. | 2026-07-28 |
| S7 | IEC 60601-1 Patient Leakage Current Limits | Official IEC publication record | Flags leakage-current validation as a medical-system requirement that can affect winding, insulation, and grounding choices. | Official record Exact limits depend on applied-part type, edition, amendments, and test condition; verify in the purchased standard. | 2026-07-28 |
| S8 | Internal supplier-history planning benchmark | Internal manufacturing estimate | Uses historical supplier quote cycles to flag 12-16 week exposure for non-catalog reducers, encoders, and magnetic materials. | Internal planning record Not an external market statistic and not a binding quote; confirm every long-lead item with named suppliers during DFM. | 2026-07-28 |