Where losing something isn't an option.

Questions people ask

Short answers to the questions that come up in almost every conversation.

Can you monitor benchtop incubators properly?

Yes. XiltriX designed probes and adapters that fit specific benchtop models, including the Esco Miri and Miri TL, CooperSurgical G185 and G210+, Merck Geri and Origio BT37, so the measurement is taken where the sample actually is.

Can you monitor equipment we already own?

In almost all cases, yes. Equipment is monitored independently, with our own sensors, rather than by trusting the device's internal readout. Where a device already provides a suitable output or contact, that can be brought in as well, including digital integration with Lighthouse particle counters.

Do you supply validation documentation?

Yes: URS and functional specification for design qualification, IQ documents recording the system as built, an OQ protocol with printed test evidence, and PQ procedures for recurring proof in normal use. Together they form the validation report you present at an audit.

Is XiltriX only for large sites?

No. Installations run from a single IVF laboratory with a handful of incubators to hospital estates and multi-site pharmaceutical operations under one contract.

How does a project start?

With a survey. A consultant walks the lab with you, lists the equipment that carries risk, and decides per device what has to be measured and where. That produces the sensor set, the alarm schema and the basis for the validation documentation.