| Flexible general-purpose tube | 1.0–6.0 mm | 1.0–2.0 mm | 50–60 Shore A | Approximately −60 to 200°C | Translucent or clear; low-odor platinum-cured silicone | Fluid transfer, laboratory lines, dispensing equipment, and low-pressure pneumatic connections | Suitable when formulation and use conditions comply | Confirm lot-specific test report | Confirm biological evaluation scope | Food-contact declaration, formulation statement, extractables information, and batch traceability |
| Thin-wall precision tube | 0.5–3.0 mm | 0.5–1.0 mm | 50–70 Shore A | Approximately −60 to 180°C | Clear or translucent; low odor after post-curing | Peristaltic pumps, analytical instruments, dosing systems, and compact fluid paths | Applicable only to qualifying food-contact formulations | Verify USP Class VI test method and report | Not automatically medical-device compliant | Dimensional inspection record, curing process information, USP test report, and change-control statement |
| High-flexibility pump tube | 2.0–12.0 mm | 1.5–3.0 mm | 40–55 Shore A | Approximately −50 to 180°C | Translucent; low odor; optimized for repeated flexing | Peristaltic pumping, beverage dosing, laboratory pumping, and flexible connections | Use only with documented food-contact compliance | Confirm suitability for repeated compression | Assess mechanical and biological requirements separately | Fatigue-life data, bore-collapse data, extractables profile, and cleaning compatibility statement |
| Reinforced pressure tube | 3.0–25.0 mm | 2.0–5.0 mm plus reinforcement | 60–80 Shore A | Approximately −50 to 180°C | Translucent outer silicone with textile reinforcement; low odor | Higher-pressure transfer, filling equipment, washdown systems, and industrial fluid handling | Check whether reinforcement materials are covered | Whole-tube construction must be evaluated | Evaluate all patient-contacting and extractable materials | Pressure and burst data, reinforcement material declaration, sterilization compatibility, and compliance reports |
| High-temperature tube | 2.0–20.0 mm | 1.5–4.0 mm | 50–70 Shore A | Approximately −60 to 220°C, application dependent | Clear or translucent; low odor after controlled post-curing | Hot-air lines, thermal processing equipment, laboratory heating systems, and high-temperature fluid transfer | Food-contact limits depend on time, temperature, and medium | Confirm thermal aging and extractables data | Sterilization and aging effects require evaluation | Thermal aging report, maximum-use-temperature statement, extractables data, and cleaning validation information |
| Medical and bioprocess tube | 1.0–25.0 mm | 1.0–4.0 mm | 45–70 Shore A | Approximately −50 to 200°C, depending on design | High-clarity or translucent; platinum-cured and low odor | Single-use assemblies, laboratory bioprocessing, pharmaceutical transfer, and medical fluid pathways | FDA food-contact status does not equal medical approval | Specify USP Class VI test evidence where required | Define applicable ISO 10993 endpoints for the intended contact | Biocompatibility evaluation, sterilization validation, extractables and leachables data, and material-change notification |