In my humble (but dare I say, experienced) opinion, minor items of test kit like this need only be referred to a master calibrated unit.
Put simply, surely "For Indication Only" is sufficient for something like a phototherapy output meter? Part of the biomed's
raison d'ĂȘtre is a basic understanding of the clinical use of the kit, and being able to prioritise the work accordingly (and the spending of both time and money on it).
What will it be next:- sending away 6-inch steel rules for calibration?

... we get FOI requests coming in, as we do on a regular basis "when was this done , when was that done" ...
Freedom of Information? What's this ... spurious demands from unhappy patients (or their successors), or lawyers looking for someone to blame? Is this the Future of Biomed? I'm glad I'm out of it, to be sure!