Most density-meter selection failures are not accuracy failures. The instrument meets its specification and still does not do the job, because the principle was wrong for the process. The most expensive high-accuracy meter in the wrong service will not run stably, and no amount of recalibration fixes it.
This guide works the other way round from a datasheet comparison. It eliminates from "cannot be used here" down to a short feasible set, and only then ranks what is left. Six steps, in order, because each one narrows the field for the next.
Why elimination beats comparison
Accuracy figures are not comparable across principles — ±0.001 g/cm³ on a clean-liquid instrument and ±1 % FS on a slurry instrument are measured against different references on different media. Comparing them directly is meaningless, and a selection process that starts there tends to arrive at an instrument that is precise in a laboratory and unusable in the plant. Constraints, unlike accuracy claims, are objective: either the pipe can be tapped or it cannot.
Before you start
Have these to hand, because every step needs them: a process flow diagram with the candidate measuring point marked, the medium's composition and its normal and upset range, line size and material, temperature and pressure, the area classification, and what the reading will actually control. That last one is asked least and matters most — a measurement feeding a trend display and one closing a dosing loop are not the same specification.