Auto Refractometer Portable, Ophthalmic Equipments

Customization: Available
Classification: Physiological Functions of Diagnosis and Monitoring Equipment
Type: ECG

Product Description

Basic Information
Model NO.
MED-AutoSight 900
Certification
CE, FDA, ISO13485
Dimensions
200mm×80mm×270mm
Electrical Safety
Battery Charger (Class I), Main Unit (Internally)
Laser Safety
Laser (Class I), Wavelength 850nm
Cylindrical(C)
-3.00d~0.00d
Axis(a)
0°~180°
Production Capacity
1000/Month
Product Description
Auto Refractometer Portable Handheld Vision Screener

Application: This product is used for preliminary determination of adults' or children's refractive error. The result of this product is used for vision screening only. It cannot replace a comprehensive eye exam.

Technical Specifications
Item Range Interval Tolerance
Spherical (S) Myopia Mode -9.00D~ +2.50D 0.25D ±0.50D or ±20%
Normal Mode -6.00D ~ +8.00D
Cylindrical (C) -3.00D~0.00D 0.25D ±0.50D or ±20%
Axis (A) 0°~180° ±5°

Working Principle: The working principle of this vision screener is based on Hartmann-Shack wavefront sensor. The internal light source is focused to the retina by the refractive media of the eye and reflected back to the device. The diopter of the patient is obtained through calculation of the detected signal.

Product Gallery & Categories
Frequently Asked Questions
What is the main function of the AutoSight 900?
The AutoSight 900 is a handheld vision screener designed for the preliminary determination of refractive errors in both adults and children, making it ideal for rapid vision screening.
Does this device provide a final prescription for glasses?
No, the results are intended for vision screening purposes only. It is a preliminary tool and cannot replace a comprehensive eye examination performed by a professional.
What technology is used for the measurements?
The device utilizes the Hartmann-Shack wavefront sensor technology, which calculates diopter by detecting signals reflected from the retina.
Is the laser used in the device safe?
Yes, the device is classified under Laser Safety Class I with a wavelength of 850nm and power less than 250μW, ensuring safe use during screenings.
What are the measurement ranges for myopia and hyperopia?
In Myopia Mode, the spherical range is -9.00D to +2.50D. In Normal Mode, the range extends from -6.00D to +8.00D.
What is the battery and electrical safety rating?
The battery charger is Class I, and the main unit is internally powered, meeting standard medical electrical safety requirements.

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