The Mayamed MY-S130H-2 is a Class II portable medical ultrasound therapy device designed to reduce pain and promote healing in soft tissues. It is intended for use in rehab centers, hospitals and, with appropriate guidance, home health care.
The device delivers therapeutic ultrasound waves that can increase local blood flow, reduce muscle tension, and support tissue healing. It provides a non‑invasive approach to address muscular pain, joint discomfort and soft tissue injuries. Clinical use and results depend on the condition treated and treatment parameters.
The product is described as a therapeutic ultrasound device; some materials also reference shockwave therapy concepts. If you need a dedicated shockwave (radial/focused) system, confirm the exact therapy modality and technical specifications with the manufacturer or the device manual before purchase.
It is designed for use in rehabilitation centers, hospitals and home settings. Home use should be done under the direction of a qualified healthcare professional and after learning proper application techniques from the user manual or clinician.
Healthcare professionals (physiotherapists, physicians, trained clinicians) should operate the device for clinical treatments. Patients may use it at home if trained and following a healthcare provider's instructions and the device's user manual.
Model: MY-S130H-2. Product type: medical ultrasound therapy device. Material: durable ABS housing. Color: white. Function: reduces pain and promotes healing. For full technical specs (frequency, intensity, power requirements) consult the product manual or manufacturer.
Yes. Common contraindications for therapeutic ultrasound include use over malignancies, active infections, open fractures or wounds, areas with impaired sensation, over the eyes or reproductive organs, and directly over implanted electronic devices (e.g., pacemakers). Do not use over areas with deep venous thrombosis or hemorrhagic conditions. Always consult the device manual and a healthcare professional before use.
Therapeutic ultrasound is generally contraindicated over the abdomen and pelvic regions during pregnancy. Pregnant people should consult their healthcare provider before any treatment.
Use on children should be performed only under the supervision of a qualified healthcare professional. Dosage and treatment parameters will differ from adults and should be prescribed by a clinician.
Treatment duration and frequency vary with the condition and clinician guidance. Typical sessions for therapeutic ultrasound often range from about 5 to 15 minutes per treatment area, with treatments commonly repeated 1–3 times per week. Follow the treatment plan prescribed by your healthcare provider and the instructions in the user manual.
The product description does not specify power source or battery details. Because it is portable, it may be mains-powered or battery/rechargeable. Check the product manual or contact the seller/manufacturer to confirm power requirements and battery options.
Wipe the ABS housing and probe with a soft cloth dampened with mild detergent or a manufacturer‑approved disinfectant. Do not immerse the device or probe in liquid. Inspect cables and connectors regularly for damage. Refer to the user manual for specific cleaning agents, probe care and storage recommendations.
The description does not list specific accessories. Typical packages for ultrasound therapy devices may include the treatment probe/transducer, power adapter or cable, coupling gel, user manual and a carrying case. Confirm included items with the seller or product listing.
Warranty and service terms are not provided in the basic description. Check with the seller or manufacturer for warranty length, what it covers, and how to obtain repair or technical support. Keep purchase documentation for warranty claims.
The product is described as a Class II medical device, indicating regulatory classification in some jurisdictions. For specific certifications (e.g., FDA 510(k), CE marking, local regulatory approvals), consult the manufacturer or product documentation and verify compliance with local regulations before clinical use.
Discover our latest orders