Pronto-7 — with rainbow 4D™ Technology — for noninvasive and quick spot-checking of total haemoglobin (SpHb®), SpO2, pulse rate, and perfusion index
A New Solution for Haemoglobin Spot-Check Testing
Traditional invasive lab testing provides delayed results and requires a painful needle prick and time consuming blood draws.
The Pronto-7 offers noninvasive and quick spot-check testing of total haemoglobin (SpHb), SpO2, pulse rate, and perfusion index, which may provide the following benefits:
Clinician
- > Facilitates timely patient assessment
- > Reduces the need to wait for lab results
Staff
- > Easy to use — reduces training time and improves efficiency
- > Decreases risk of accidental needle pricks and exposure to blood-borne pathogens
- > Requires no lab consumables or waste disposal
Patient
- > Reduces painful needle pricks and time-consuming blood draws
- > Enables immediate face-to-face counselling with clinician
Four Simple Steps
Select sensor size
Place sensor on finger
Press test button
Obtain results
Automatically saved — option to print,
e-mail, or manually record
SpHb Analytical Performance
In 11,335 comparisons of SpHb and invasive haemoglobin (tHb) measurements from a laboratory reference device, SpHb accuracy was as follows:1
- • -0.02 g/dL bias
- • 0.99 g/dL at one standard deviation
- • Between 6 - 12 g/dL, greater than 95% of SpHb readings were within 2 g/dL of the laboratory tHb value
- • Between 12 - 18 g/dL, greater than 95% of SpHb readings were within 2 g/dL of the laboratory value
Please note: These results were obtained following a specific protocol, in which all Directions for Use were followed and SpHb measurements were compared to validated laboratory reference measurements. Differences in results may be caused by many factors, such as those explained in Masimo’s Directions for Use. Some independent researchers have conducted their own testing and obtained similar results, while other researchers have reported larger differences when comparing SpHb measurements to laboratory measurements.
1 Masimo FDA 510(k) Submission Data using normal sensitivity mode.
* 510(k) Clearance Pending.






