Protect the clinical load
Online double-conversion with output PF 1 and THDi <3% isolates monitors, analyzers and ventilators from grid noise and transfer events.
Engineering teams own the uptime. XGW gives you online UPS and LiFePO4 batteries sized for ICU, laboratories and ventilation — with wide-input models that ride through unstable grids and thermal designs proven at 45–50 °C.
Online double-conversion with output PF 1 and THDi <3% isolates monitors, analyzers and ventilators from grid noise and transfer events.
Wide-input UPS accepts sagging or drifting mains; LiFePO4 strings run 24/7 in 45–50 °C ambients without the watering and mid-life swaps VRLA demands.
Send the load list and required minutes; we size the string (Ah ≈ load × hours ÷ bus voltage ÷ efficiency) and confirm the BMS protocol with the host UPS.
1–600 kVA for wards & labs
View product →LiFePO4 48V–409V
View product →central modular UPS
View product →XGW UPS lithium battery and critical-power deployment.
Read case →XGW UPS lithium battery and critical-power deployment.
Read case →Middle East, Africa, Latin America
We help hospital engineering specify runtime by load, match the DC bus and BMS protocol to the existing UPS, and deliver drop-in LiFePO4 strings (48V–409V) with UN38.3 certification. OEM/ODM and spare support available.
37 senior R&D engineers. OEM/ODM from 500 units. Samples in 3–7 days. Send us your load list and backup requirement — we return a sized configuration.
Get a Quote WhatsApp UsXGW UPS and battery systems are general-purpose critical-power products, certified to IEC 62040 (UPS) and UN38.3 (battery transport). They are not medical devices and are not certified to IEC 60601 or any medical-equipment standard. Before deploying in patient-care areas, confirm compatibility with the specific medical device against the device manufacturer’s published power specifications and your local electrical and regulatory requirements. XGW confirms UPS/battery fit (DC-bus voltage, charge profile, communication protocol) when given the UPS model — the medical-device compatibility decision remains with the equipment manufacturer and the facility.