Topography and Dry Eye Analysis 
Anterior Segment Analysis 
Slit Lamp / Documentation 
Autorefractor 
Myopia Master® 
Perimetry 
Tonometer 
Visual Test Equipment 
Vitreoretinal Surgery 
Trial Frames 
Binocular Loupes 
Perimetry 
Dry Eye 
The PARK 1® combines a non-contact pachymeter, auto-refractometer and keratometer in one unit. In addition to the objective refraction, the keratometer values and the pachymetry can be determined with precision in a matter of seconds with the PARK 1®.
The integrated patient data management system facilitates the organization of the data and ensures patient-friendly contact lens fitting. Thanks to its space-saving, compact design, this award-winning unit is ideal for use in every ophthalmology practice.
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OCULUS PARK 1® |
| Measuring range | 200 bis 1 200 μm |
| Number of evaluated measuring points | 600 |
| Measuring time | Approx. 1 sec. |
| Light source | Blue LEDs (455 nm UV-free) |
| Corneal vertex distance (CVD) | 0; 10.5; 12; 13.75; 15; 16.5 mm |
| Sphere | -20 to +22 dpt (CVD = 12 mm) (choice of 0.01-; 0.12- or 0.25 dpt increments) |
| Cylinder | 10 dpt (CVD = 12 mm) (choice of 0.01-; 0.12- and 0.25 dpt increments) |
| Axis | 0° to 180° (in 1° increments) |
| Smallest measurable pupil diameter | 2.5 mm |
| Fixation image | Hot air balloon in a landscape |
| Measuring range | 9 to 99 dpt 3 to 38 mm |
| Accuracy | ± 0.1 dpt |
| Reproducibility | ± 0.1 dpt |
| Far PD | 20 to 80 mm (in 1 mm increments) |
| Corneal diameter measuring range | 10 to 14 mm (in 0.1 mm increments) |
| Pupil diameter measuring range | 1 to 8 mm (in 0.1 mm increments) |
| Auto alignment | Automatic height alignment (y-direction) |
| Auto release | Automatic measurement release |
| Working distance | Approx. 36 mm |
| Dimensions H x W x D | 500 x 265 x 538 mm |
| Weight | 12 kg |
| Power supply | 100 - 240 V AC, 50 - 60 Hz |
| Printer | Thermal printer |
| Display | TFT - LCD 5.7" (Touchscreen) |
| Interface | USB |
| Standard accessories | Printer paper, power cable, dust cover, chin rest paper, USB mini cable |
In acc. with the Medical Device Directive 93/42/EEC
The OCULUS QM system is certified in accordance with ISO 13485 and (EU) 2017/745 (MDR).
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The OCULUS QM system is certified in accordance with ISO 13485 and (EU) 2017/745 (MDR). |
