Online UPS for ICU & Laboratory Equipment

ICU monitors, infusion systems and laboratory analyzers are sensitive to the things a weak grid does: sags, swells, frequency drift and the brief break of a line-interactive transfer. XGW online double-conversion UPS eliminates those events at the source — the load runs on the inverter continuously, so it never sees the raw grid. This is why online topology is the standard choice for ICU and lab environments.

What online double-conversion does for ICU and lab loads

Why lab equipment needs the same protection

Centrifuges, refrigerated units and analytical instruments draw sharp inrush when motors or compressors start. An online UPS sized with inrush margin holds voltage through the surge instead of tripping, and the battery (up to 6C peak discharge on XGW LiFePO4) carries the spike without sagging the way a VRLA string can.

XGW online UPS for ICU and lab

Industrial & Tower UPS 1–600 kVA

Single-phase 1–20 kVA for bedside and bench loads; three-phase tower/rack to 600 kVA for whole-ward or building service. >96% efficiency, full DSP control, wide input range.

Modular Three-Phase UPS 50–720 kVA

N+X hot-swappable redundancy for central ICU/lab power: a module fault or service window never drops the load. Scales to 2.0 MVA as the facility grows.

Pair either with the LiFePO4 UPS battery (48V–409V) for long, maintenance-light runtime and protocol-matched BMS telemetry to the building management system.

Deployment notes

Protecting an ICU or lab?

Send the load list and required runtime. 37 senior R&D engineers, OEM/ODM from 500 units, samples in 3–7 days.

Get a Quote WhatsApp Us

Compliance & scope note

XGW 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. This page describes power-protection principles and XGW product capabilities; it is not a statement of compatibility with any specific ICU or laboratory device. Compatibility must be confirmed against the device manufacturer’s published power specification and your local electrical and regulatory requirements before deployment in patient-care or calibration-sensitive areas.