NEW
NEW
Strongly agrees with subjective refraction
Modern operator and patient experience
Intuitive design and controls
QuickSee Free Pro’s combination of the open view design, wavefront aberrometry, and innovative measurement algorithms produces clinically accurate autorefraction results, comparable to the best desktop autorefractors but in a compact, handheld format.
The patented PlenOptika Wavefront Refraction Engine™ precisely determines low-order refractive errors, demonstrating excellent agreement with subjective refraction.
QuickSee Free Pro’s technology has been clinically-evaluated in five IRB-based studies and documented in many peer-reviewed publications and conference abstracts. QuickSee Free has FDA Class I 510(k) exempt medical device registration.
QuickSee Free Pro’s UI is clean, intuitive, and robust
| AUTOREFRACTOR | |
| Pupil size | 2 to 8 mm |
| Intended patient population | >= 3 years |
| Accommodation control | Open view, Fogging lens (optional) |
| Cycloplegia requirement | None |
| Dilation requirement | None |
| Illumination requirement | None |
| Acquisition time | 5, 10 seconds |
| Spherical range | -13D to +10D, increments of 0.01D, 0.125D, 0.25D |
| Cylindrical range | -8D to +8D, increments of 0.01D, 0.125D, 0.25D |
| Axial range | 0–180º, increments of 1º, 5º, 10º |
| Base technology | Wavefront aberrometry |
| KERATOMETER | |
| Radius of curvature | 5 to 12 mm in 0.01 mm increments |
| Corneal astigmatism | 0 D to +/- 8 D (R 5 to 12mm) |
| Center | Diameter 3.2 mm at Radius of curvature 8 mm |
| Display properties | 2.4-inch LCD, capacitive touch screen, readable outdoors, true color (65,536 colors) |
| Charger properties | USB-C medical grade wall adapter, AC 100 to 240V, 50/60 Hz |
| Battery | 6 hours continuous use +/– 1 hour (10,000 mAh Li-ion); 3 hours charge time (5% - 75%); 5 hours charge time (0% - 100%); IEC 62133-2:2017 certified |
| Calibration | Factory calibrated; no field calibration needed |
| Measurement capacity | Measurement storage capacity: > 10,000 measurements |
| Regulatory classification (medical device) | Class I FDA (USA), Class IIa Product CE, MDR Compliant, Class IIa, UKCA, MDR 2002 Compliant |
| Laser safety | Class 1, IEC 60825-1:2014 certified |
| Weight | < 750 grams / 1.65 lbs |
| Dimensions | 30 cm (H) x 5.5 cm (W), 18 cm (L) |
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