2.1
Three CE‑marked point‑of‑care coagulometers for self‑monitoring coagulation status were identified during scoping as being relevant to this assessment. One of these coagulometers, the ProTime microcoagulation system, was included in the assessment but has been removed from this guidance because it is no longer available to the NHS and its successor model is not intended for patient self‑monitoring. Additional details of the coagulometers included in the guidance are provided in section 4.