{"title":"DVT Prevention System","description":"\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eDVT Prevention System\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eProfessional intermittent pneumatic compression solutions designed to support venous circulation and DVT prevention. The system provides adjustable pressure therapy with comfortable compression for hospitals, clinics, rehabilitation centers, and home-care applications.\u003c\/span\u003e\u003c\/p\u003e","products":[{"product_id":"deep-vein-thrombosis-dvt-prevention-and-treatment-productqj-b100","title":"Deep Vein Thrombosis (DVT) Prevention and Treatment Product (QJ-B100)","description":"\u003ch1\u003e\u003cspan\u003eDeep Vein Thrombosis (DVT) Prevention and Treatment Product(QJ-B100)\u003c\/span\u003e\u003c\/h1\u003e\n\u003ch3\u003e\u003cspan\u003eTechnical Specifications\u003c\/span\u003e\u003c\/h3\u003e\n\u003col start=\"1\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eScreen and Operation\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003e5-inch capacitive touchscreen\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eBased on the T5L1 chip\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDGUS II operating system\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eResolution: 480 × 854\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003e16.7 million colors\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eTreatment Modes\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eManual Treatment\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eStandard Treatment\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eTreatment Pressure\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eMaximum treatment pressure: 300 mmHg\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eMinimum treatment pressure: 0 mmHg\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003ePressure adjustment accuracy: 1 mmHg\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eRelevant parameter documentation shall be provided as required by the applicable national regulatory authority.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eTreatment Functions\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eSupports both \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eplantar foot pressure cuffs\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e and \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003ecalf pressure cuffs\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e for treatment.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eDevice Indication Functions\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDuring operation, the screen displays treatment time and pressure.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe deviation between the displayed pressure and the actual measured pressure shall not exceed ±5 mmHg.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eOverpressure warning\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eUnderpressure warning\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eFault warning\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDynamic treatment-site indication: the treatment site currently being treated flashes on the screen.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eOverpressure Protection\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device incorporates dual overpressure protection through both software and hardware safeguards.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eIn the event of overpressure, the device provides an overpressure warning and automatically releases the air pressure inside the chambers.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eUnder a single-fault condition, the system is designed to release the maximum pressure in the chambers and connecting tubing.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe pressure delivered to the limb shall not exceed 120% of the maximum treatment pressure for more than 1 second.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eRelevant parameter documentation shall be provided as required by the applicable national regulatory authority.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eFunction Control\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device is equipped with an output stop switch, allowing the treatment procedure to be interrupted at any time.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eFault Self-Inspection\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device is equipped with a fault self-inspection function.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ePulse Width and Refill Time\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdjustable pulse width: Levels 1–5\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdjustable refill time: 20–70 seconds\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ePressure Release Measures\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cp\u003e\u003cspan\u003eThe device provides pressure-release measures under the following conditions:\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ea. Manual pressure release:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eThe patient pressure can be manually released under various operating conditions. Disconnecting the ventilation tubing is sufficient to release the pressure.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eb. Completion of treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs when the preset treatment time is reached and the treatment program is completed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ec. Power interruption:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs in the event of sudden loss of power.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ed. Device fault:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs when a fault is detected and a fault warning is triggered.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ee. Temporary treatment interruption:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs when the treatment program is temporarily interrupted.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn all of the above situations, pressure release shall be completed with a single action. The time required for the patient pressure to decrease from the maximum pressure to \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e2 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e10 seconds\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003col start=\"11\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eInstallation and Mounting\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eSuitable for bedside use.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eCan also be mounted on a dedicated medical trolley.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"12\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eSafety and Pressure Resistance\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe chambers and connecting tubing shall withstand a pressure of \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e450 mmHg for 1 minute\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e without rupture or permanent (plastic) deformation.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eConnections shall remain secure without loosening or visible deformation.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe chambers and connecting tubing shall withstand sudden external forces without localized bulging or rupture.\u003c\/span\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0849\/3373\/8744\/files\/Woman_relaxing_on_sofa_2K_202609011647.jpg?v=1788254084\" alt=\"\"\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0849\/3373\/8744\/files\/Woman_using_compression_device_2K_202609011646.jpg?v=1788254085\" alt=\"\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"QIJIA MEDICAL","offers":[{"title":"Default Title","offer_id":50408553152760,"sku":"QJ-B100","price":1790.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0849\/3373\/8744\/files\/DSC_3612.jpg?v=1788254161"},{"product_id":"deep-vein-thrombosis-dvt-prevention-and-treatment-productqj-b300","title":"Deep Vein Thrombosis (DVT) Prevention and Treatment Product (QJ-B300)","description":"\u003ch1\u003e\u003cspan\u003eDeep Vein Thrombosis (DVT) Prevention and Treatment Product(QJ-B300)\u003c\/span\u003e\u003c\/h1\u003e\n\u003ch3\u003e\u003cspan\u003eTechnical Specifications\u003c\/span\u003e\u003c\/h3\u003e\n\u003col start=\"1\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eScreen and Operation\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003e5-inch capacitive touchscreen\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eBased on the T5L1 chip\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDGUS II operating system\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eResolution: 480 × 854\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003e16.7 million colors\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eTreatment Modes\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe system provides five treatment modes: \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eManual Treatment, Gradient Treatment, Standard Treatment, Advanced Treatment, and Customized Treatment\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e, with at least 30 treatment programs available.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ea) Manual Treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAll treatment parameters can be adjusted manually, allowing the user to select appropriate parameters for treatment. The treatment pressure output error shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±3 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eb) Gradient Treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eOnly the pressure of the distal chamber needs to be set. The pressure of each subsequent chamber toward the proximal end decreases by \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e15 mmHg\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e sequentially. The maximum set pressure is \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e150 mmHg\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e. The treatment pressure decreases by 15 mmHg from the distal chamber to the proximal chamber. The treatment pressure output error shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±3 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ec) Standard Treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAll chambers operate at the same pressure, with different treatment modes available according to different inflation sequences. The treatment pressure output error shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±3 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ed) Advanced Treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eBased on Standard Treatment, this mode provides a function that allows the chamber corresponding to an injured area to remain unpressurized. The treatment pressure output error shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±3 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ee) Customized Treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eHealthcare professionals can create customized treatment programs according to individual patient requirements and can store treatment programs for at least \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e15 patients\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e. The treatment pressure output error shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±3 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eTreatment Pressure\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdjustable treatment pressure range: \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e0–300 mmHg\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eOperating Time\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdjustable treatment time: \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e0–9999 minutes\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eDual Treatment Functions\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device provides both:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eLow-pressure gradient compression for antithrombotic applications\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eHigh-pressure air-wave massage\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eSeparate \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003esemi-wrap and full-wrap limb pressure cuffs\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e are provided for the corresponding treatment functions.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eTreatment-site selection is supported, including the function to exclude an injured area or designated treatment area from pressurization.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eDevice Indication Functions\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDuring operation, the screen displays treatment time and pressure.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe deviation between the displayed pressure and the actual measured pressure shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±5 mmHg\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eOverpressure warning\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eUnderpressure warning\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eFault warning\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eDynamic treatment-site indication: the treatment site currently being treated flashes on the screen.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eOverpressure Protection\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device incorporates dual overpressure protection through both software and hardware safeguards.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eIn the event of overpressure, the device provides an overpressure warning and automatically releases the air pressure inside the chambers.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eUnder a single-fault condition, the system is designed to release the maximum pressure in the chambers and connecting tubing.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe pressure delivered to the limb shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e120% of the maximum treatment pressure for more than 1 second\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eFunction Control\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device is equipped with an output stop switch, allowing the treatment procedure to be interrupted at any time.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eFault Self-Inspection\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe device is equipped with a fault self-inspection function.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ePulse Width and Refill Time\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdjustable pulse width: \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e0–20 seconds\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eWhen the pulse width is set to 5 seconds, the error shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e±5%\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e of the set value.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAdjustable refill time: \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e0–120 seconds\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"11\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eInflation Speed\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003e12-level adjustable inflation speed: \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eLevels 1–12\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eAt Level 12, the maximum inflation speed, the time required to fully inflate a single air chamber in Gradient Treatment mode shall be \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eless than 10 seconds\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"12\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ePressure Release Measures\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cp\u003e\u003cspan\u003eThe device provides automatic pressure release under the following conditions:\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ea) Manual pressure release:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eThe patient pressure can be manually released under various operating conditions. Disconnecting the ventilation tubing is sufficient to release the pressure.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eb) Completion of treatment:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs when the preset treatment time is reached and the treatment program is completed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ec) Power interruption:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs in the event of sudden loss of power.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ed) Device fault:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs when a fault is detected and a fault warning is triggered.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ee) Temporary treatment interruption:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eAutomatic pressure release occurs when the treatment program is temporarily interrupted.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn all of the above situations, pressure release shall be completed with a single action. The time required for the patient pressure to decrease from the maximum pressure to \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e2 kPa\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e10 seconds\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003col start=\"13\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eInstallation and Mounting\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eSuitable for bedside use.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eCan also be placed on a dedicated medical trolley.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"14\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ePressure Resistance\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe chambers and connecting tubing shall withstand a pressure of \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e450 mmHg for 1 minute\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e without rupture or permanent (plastic) deformation.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eConnections shall remain secure without loosening or visible deformation.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe chambers and connecting tubing shall withstand sudden external forces without localized bulging or rupture.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"15\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eAir Tightness\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe air chambers and connecting tubing shall provide good air tightness.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eWhen maintained at the device's specified maximum output pressure for \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e1 minute\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e, the pressure drop of the air chamber shall not exceed \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e10%\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"16\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eConnection Identification\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe connecting tubing shall be equipped with a mechanism or identification mark to prevent incorrect connection.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"17\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eScreen Control Functions\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ea) Screen Lock Function:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eDuring operation, tapping the lock icon locks the treatment parameters to prevent accidental operation. The parameters can be adjusted after tapping the unlock icon.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eb) Screen Brightness and Night Mode:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eScreen brightness is adjustable to at least \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e8 levels\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e, with support for Night Mode.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003ec) Automatic Screen-Off Function:\u003c\/span\u003e\u003c\/strong\u003e\u003cbr\u003e\u003cspan\u003eThe automatic screen-off time can be set from \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003e1 to 60 minutes\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e. When enabled, the screen automatically turns off after the preset time.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cem\u003e\u003cspan\u003eSupporting documentation shall be provided in the response documents. Failure to provide such documentation shall be considered a deviation.\u003c\/span\u003e\u003c\/em\u003e\u003c\/p\u003e\n\u003col start=\"18\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eElectrical Safety and EMC Compliance\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eComplies with \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eGB 9706.1-2020, Medical Electrical Equipment – Part 1: General Requirements for Basic Safety and Essential Performance\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eComplies with \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eYY 9706.102-2021, Medical Electrical Equipment – Part 1-2: General Requirements for Basic Safety and Essential Performance – Collateral Standard: Electromagnetic Compatibility – Requirements and Tests\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"19\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eLimb Pressure Cuffs\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eA \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003ethree-chamber split limb pressure cuff\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e is used in Gradient Treatment mode.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eA \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003efull-leg limb pressure cuff\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e is used in other treatment modes.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eBoth reusable and single-patient-use versions are available as optional configurations.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe supplied limb pressure cuffs must have a \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eseparate medical device registration certificate\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"20\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eBlood Refill Detection Technology\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eEquipped with blood refill detection technology.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003ePatent certificate documentation shall be provided as supporting evidence.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"21\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eISO 13485 Certification\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eA valid \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eISO 13485 Quality Management System Certificate\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e shall be provided.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"22\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eUnique Device Identification (UDI)\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eEach device is incorporated into the global \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eUnique Device Identification (UDI)\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e system.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eEvery device is assigned a unique medical device UDI code.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe UDI can be parsed through the \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eIDCODE platform\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e to access detailed product information, facilitating product verification and information retrieval.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"23\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eCE Certification\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eA valid \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eCE Certificate\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e shall be provided.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003col start=\"24\"\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cstrong\u003e\u003cspan\u003eSupporting Documentation\u003c\/span\u003e\u003c\/strong\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ol\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cp\u003e\u003cspan\u003eThe supporting documentation referred to in the response documents consists of the technical requirements specified in the \u003c\/span\u003e\u003cstrong\u003e\u003cspan\u003eproduct registration certificate and its attachments\u003c\/span\u003e\u003c\/strong\u003e\u003cspan\u003e.\u003c\/span\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0849\/3373\/8744\/files\/DVT_Prevention_Devices_bf618b23-6978-44a1-aa69-af4f8d65f2a6.jpg?v=1788255258\" alt=\"\"\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"QIJIA MEDICAL","offers":[{"title":"Default Title","offer_id":50408959279352,"sku":"QJ-B300","price":1300.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0849\/3373\/8744\/files\/DSC_3612_581c44b2-5b45-4d81-8a37-cb4e4627c632.jpg?v=1788255348"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0849\/3373\/8744\/collections\/DVT_Prevention_Devices.jpg?v=1788254270","url":"https:\/\/shop.jnqijia.com\/collections\/dvt-prevention-system.oembed","provider":"QIJIA Medical","version":"1.0","type":"link"}