So the reason proteins don't have "blind tests" is because of the complexity (and expense) of analyzing a broad spectrum of possibilities. Basically, you have to know what you're looking for, and things like dimer (two hgh proteins attached) and other similar, but not exactly the same, proteins will be detected at the same time.
Pharma has to identify every impurity and ensure they're not something potentially dangerous. That kind of in depth analysis is not practical at a reasonable cost.
So there's 5% of unidentified "stuff".
Statistically, the most likely "impurity" would be aggregates(or aggregate inducing defective/fragmented protein chains, "seeds"). Dimer is a well known type of aggregate, but they can get much larger. Thousands of times larger in some cases.
So if you chose to use this batch, I would use a .22um PES filter, which will eliminate the largest aggregates, since those are the ones most likely to cause issues (an immune response). Do that and it'll probobly be fine.