SBM IDRA X Dry Eye Diagnostic Platform

Description

The SBM Sistemi IDRA X is an advanced ophthalmic platform designed to support comprehensive examination of the tear film, meibomian glands and ocular surface.

Its integrated acquisition system combines a 20-ring Placido disc with an 8-megapixel camera, automatic and manual focusing, and color and infrared imaging. Infrared, white and blue LED illumination supports different ocular-surface acquisition modes without requiring direct contact with the eye.

IDRA X captures single images, multishot sequences and video. Standard photographs are recorded at 2592 × 1944 pixels in JPEG format, while analyzed images can be digitally upscaled to a published resolution of 23 megapixels.

Depending on the installed software package and licensed examinations, the platform can support dry-eye workflows such as tear-film interferometry, noninvasive tear-breakup time, tear-meniscus evaluation, meibography, blink assessment, ocular-redness classification and anterior-segment documentation.

Its desktop design, adjustable 60–90 mm working distance and USB 3.0 workstation connection facilitate integration into specialized ophthalmology, optometry and dry-eye practices.

Key Features

Dedicated dry-eye and ocular-surface platform
Noncontact optical acquisition
20-ring Placido system
8 MP camera
2592 × 1944-pixel photographs
Analyzed images upscaled to 23 MP
Color and infrared imaging
Automatic and manual focusing
Single-shot, multishot and video acquisition
Variable ISO control
Infrared, white and blue LED illumination
Adjustable 60–90 mm working distance
USB 3.0 workstation connection
Integrated chin rest and patient-positioning system
Supports photographic and video documentation
Designed for longitudinal examination comparison
IEC 60601-1-2:2015 electromagnetic compatibility

Supported Clinical Workflow

Depending on the software and license supplied, IDRA X may support:

Tear-film interferometry
Lipid-layer evaluation
Noninvasive tear-breakup time—NIBUT
Tear-film stability mapping
Tear-meniscus evaluation
Infrared meibography
Meibomian gland assessment
Blink-quality analysis
Eyelid-margin and blepharitis documentation
Bulbar-redness classification
Pupillometry
White-to-white measurement
Anterior-segment imaging
Dry-eye reports and follow-up comparison

Technical Specifications

Placido rings: 20
Camera resolution: 8 MP
Photo resolution: 2592 × 1944 pixels
Photo format: JPEG
Upscaled analyzed-image resolution: 23 MP
Acquisition modes: Single shot, multishot and video
Focus: Automatic and manual
ISO control: Variable
Image modes: Color and infrared
Illumination: Infrared, white and blue LEDs
Working distance: 60–90 mm from the center of the Placido disc
Data output: USB 3.0
Input voltage: 100–240 V
Internal operating voltages: 24 V, 5 V and 3.3 V
Electromagnetic compatibility: IEC 60601-1-2:2015
Dimensions: 40 × 51 × 47 cm (L × H × D)
Weight: 12 kg

Optional Accessories

The manufacturer publishes the following accessories, whose inclusion must be confirmed in the quotation:

Protective device cover
Ophthalmic instrument table
7 m powered USB 3.0 extension cable
Preconfigured mini computer
Transillumination everter

Published Mini Computer Configuration

Intel Core i7-12700 processor
16 GB DDR4 RAM
512 GB SSD
Intel UHD 770 graphics
Ethernet, Wi-Fi 6 and Bluetooth 5.2
Windows 11 Pro

Recommended Applications

Dry-eye assessment
Tear-film evaluation
Meibomian gland examination
Meibomian gland dysfunction assessment
Tear-film stability analysis
Tear-volume evaluation
Eyelid and blink assessment
Contact-lens evaluation and follow-up
Preoperative ocular-surface examination
Treatment documentation
Longitudinal comparison
Patient education

Important Note

The exact examinations, automatic measurements, reports and software functions must be confirmed according to the IDRA X license and configuration included in the quotation. The computer, table, cover and other accessories may be sold separately.

IDRA X is intended for use by qualified eye-care professionals. Its images, measurements and software-generated results must be interpreted together with the complete clinical examination and do not independently constitute a diagnosis.