The OCULUS Smartfield is a compact visual field device purposefully optimized for monitoring functional impairment in glaucoma. Based on an ultra-high-luminance LCD screen it performs standard automated perimetry of the central visual field and beyond. Despite its small size, the Smartfield perimeter offers a comprehensive clinical solution in visual field testing for any glaucoma practice.
Programs | Pre-defined glaucoma, macula, screening and neurological tests user-defined tests |
Test patterns | 30x24 (SPARK), 24-2, 10-2, customized patterns |
Strategies | Threshold strategies: SPARK Precision, SPARK Quick, OCULUS Fast Threshold, Full Threshold (4/2), Age-adapted suprathreshold screening (2-zone, 3-zone) |
Examination speed | Adaptive/fast/normal/slow/user-defined |
Fixation control | Through central threshold, Heijl-Krakau (using the blind spot), live video image |
Result display | Greyscale, dB values (absolute/relative), symbols, probabilities, 3D plot |
Reports | Enhanced Glaucoma Staging System (GSS 2), Glaucoma Staging Program (GSP), PATH function-structure analysis, Threshold Noiseless Trend (TNT) progression report |
Stimulus viewing distance | Infinity |
Max. eccentricity horizontal/vertical | 30°/25° (60°/50° with fixation shift) |
Stimulus size | Goldmann III |
Stimulus colour | White |
Stimulus duration | 200 ms/user-defined |
Threshold range/step | 0.8 – 3 180 cd/m2 (2.5 – 10 000 asb), 0 - 36 dB/1 dB |
Background luminance | 10 cd/m2 (31.4 asb) |
Patient positioning | Height-adjustable measuring head, adjustable chin rest, double head rest |
Software | Device control, patient management, backup and print software (Windows®) Built-in networking, easy EMR-integration, DICOM compatibility |
Dimensions (W x D x H) | 332 x 418 to 477 x 402 mm (13.1 x 16.5 to 18.8 x 15.9 in) |
Weight | 7.6 kg (16.8 lbs) |
Max. power consumption | 30 W |
Voltage | 100 - 240 V AC |
Frequency | 50 - 60 Hz |
Recommended computer specifications | Intel® CoreTM i5, 500 GB HDD, 8 GB RAM, Intel® HD Graphics, Windows® 10 |
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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