SCHWIND AMARIS Specifications

Laser type ArF Excimer laser, 193 nm, laser class 4
Beam diameter 0.54 mm Super-Gausian profile (FWHM)
Repetition Rate 500E model - 500 Hz / 750S model - 750Hz / 1050RS - 1050Hz
Beam delivery Flying spot (with Automatic Fluence Level Adjustment and Intelligent Thermal Effect Control)
Eyetracking System 1050 Hz turbo eyetracking with pupil and limbus tracking, rotation balance
Optional: 6-D active Z-axis tracking on 750S and 1050RS models only. For the 1050RS there is also the option of Latency-Free tracking using predictive algorithms
Advanced Cyclotorsion Control
(Static and Dynamic)
Optional: static for corneal wavefront-guided treatments
Optional: static for occular wavefront-guided treatments
Optional: dynamic for online correction
Treatment range with integrated SCHWIND-CAM PTK, PRK, TransPRK, LASEK, Epi-LASIK, LASIK, Femto-LASIK
"Abberation-Free" treatments, customised wavefront treatments based on corneal and occular wavefront data
Integrated online pachymetry Optional
Particle aspiration system Integrated
Laser arm Fixed for 500E and 90° swivelling for 750S and 1050RS
Patient bed Manual swivel to 90° with optional SW controlled motorised action
Treatment Assistant Manager Course of treatment can be configured individually
Surgical Microscope Leica-based, stereopsis of 14°
Tube swivelling range 10° to 50°
Integrated camera beam splitter
Computer Panel PC – 21" touch screen monitor, swivelling on 2 axes
additional dot-matrix display in direct view of surgeon. Membrane keybaord with integrated mousepad
Diagnostic slit lamp Optional: swivelling on 2 axes with interchangeable slits
Integrated video camera/DVD recorder Optional
Working distance 235 mm
Voltage/power consumption 100, 110, 120, 127 VAC, 50/60 Hz, max. 20 A
208, 220, 230, 240 VAC, 50/60 Hz, max. 10.5A
Dimensions (L/W/H) including patient bed 2637 mm x 1443 (±50) mm x 1361 mm
Space requirements Optional
Weight of basic instrument (laser) 463 kg (net)
Weight of patient bed 147 kg (net)
Cooling Air cooled
Gas supply 10 l ArF premix bottle
Compliance CE conformity in accordance with Medical Device Directive (MDD) 93/42/EEC
Australian Registration ARTG ID: 148607

Optional functionality, reliability and compliance with all legal regulations can only be assured through the use of products supplied by SCHWIND – whether as single items or as a system combination.