TearScience™ LipiScan™ Dynamic Meibomian Imager
With a small footprint and user-friendly design, the TearScience LipiScan with Dynamic Meibomian Imaging (DMI) was designed to make high-definition meibography accessible for any practice.
With a small footprint and user-friendly design, the TearScience LipiScan with Dynamic Meibomian Imaging (DMI) was designed to make high-definition meibography accessible for any practice.
Key Features
High-definition meibomian imaging
Provides enhanced view of meibomian gland structure
Versatile design
Small and light weight
Maximize workflow efficiency
Easy facility integration with meibomian gland imaging in about 10 seconds
Dynamic meibomian imaging
Images for illustrative purposes only. Actual results may vary.
Dynamic Illumination
Surface lighting originates from multiple light sources to minimize reflection.
Adaptive Transillumination
Changes to the light intensity across the surface of the illuminator compensate for the lid thickness variations between patients.
Dual-Mode DMI
Dynamic Illumination offers an enhanced view of meibomian gland structure
Reference
1. TearScience LipiScan IFU, United States.
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SUMMARY OF IMPORTANT SAFETY INFORMATION Rx Only INDICATIONS FOR USE CONTRAINDICATIONS PRECAUTIONS ADVERSE EFFECTS PP2023OTH5148
FOR THE TEARSCIENCE™ LIPISCAN™ DYNAMIC MEIBOMIAN IMAGER
TearScience LipiScan Dynamic Meibomian Imager (DMI) is an ophthalmic imaging device intended for use by a physician in adult patients to capture, archive, manipulate and store digital images of the meibomian glands.
Contraindications are conditions in which the device should not be used because the risk of use clearly outweighs any benefit. No contraindications have been identified for the TearScience LipiScan.
Precautions provide information regarding any special care to be exercised by the practitioner for the safe and effective use of the device, as described below. Caution: Disinfect the surfaces of the chin rest, forehead rest and Handheld Near Infrared (IR) Lid Everter with isopropyl alcohol immediately prior to use and prior to storage to prevent cross-contamination and patient infection.
There are no known or anticipated adverse effects associated with use of this device.
