Optometry Equipment LCD Carejoy PD Pupil Meter Digital Pupilometer White Optical

Description

The design of LED light source and low power consumption, long service life of the battery;
Adopting high-precision line-shaped sensors, advanced intellectualized electronic system and digital display which allow the testing results more visible,legible and accurate;
Using mechanical hairspring to level at the reflecting point of human cornea to realize the consecutive measurement. It features direct point sampling and high accuracy of orientation;
LED light source, time of auto power off could be adjustable. There is a +2.00D lens under measuring window to make a visual compensation.
Specification:
Color:White
Range of measurement:45~82mm(total) in 0.5mm steps,22.5~41mm(each) in 0.5 steps
Step: 0.5mm
Time for Automatic Shut-off:
About 1 Minute After Stopping Operation, or Turn It off Manually
Power Supply:AA batteries(Not Include)
Dimensions:220x160x55mm
Net Weight: 0.7kg
Package Include:
1 X Digital PD Meter
FDA declaration :
Statement：The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item.
This item has been cleaned and treated according to the manufacturer's instructions.
The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods(ARTG) with the code 136606. div >
The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number：K132989
The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number：K180353
The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number：K141973
massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number：K161892