Deviations in iron levels in human blood beyond normal physiological thresholds can signify more than just iron deficiency anemia; they may also indicate serious conditions such as hemochromatosis, acute iron poisoning, active cirrhosis, or hepatitis, necessitating precise estimation of iron levels in vulnerable individuals. While bone-marrow-based detection is considered the gold standard, its procedural complexity makes it impractical. Thus, there is a critical need for alternative methods, particularly in resource-limited settings. Addressing these challenges, we introduce a paper-microfluidics integrated fast cyclic voltammetry kit capable of on-site plasma separation and simultaneous iron detection. This approach employs a single scanning rate of approximately 200 V/s across a nanomaterial-coated screen-printed electrode. The redoxactive manganese component of the nanomaterial enables rapid peak determination due to its variable oxidation states and high redox potential. Moreover, the nanomaterial-coated electrode coupled to the porous architecture of the paper matrix enhances electron transfer rates, resulting in amplified cathodic currents. The sensor exhibits high selectivity, with cyclic voltammetry demonstrating a noticeable reduction in redox potential (approximately −0.8 V) and a high limit of detection. For a reference iron concentration of 27 μmol/L, the sensor generates a current of about 110 μA with minimal background noise. It boasts a rapid response time of 0.1 s (yielding an overall sample-to-answer detection time of around 2 min) and a sensitivity of 0.3 μg/dl, making it suitable for rapid point-of-care diagnostics. Furthermore, this approach offers broader applicability beyond iron detection, providing a platform for the highly sensitive, specific, and rapid detection of various target analytes in blood plasma without requiring complex device architecture or external fields.