-40%
Portable Manual Lensmeter Optometry Machine - CE Certified Eye Care Tool
$ 147.26
- Description
- Size Guide
Description
Description:This Lensmeter and Focimeter tester is essential for testing the lens, prism refraction, cylindrical axis, and optical center of glasses. It features AC/DC dual power options for convenience. With precise readings, clear scale, and easy operation, it is ideal for glasses manufacturers, shops, and ophthalmologists. The compensating prism ensures accurate measurements for both lenses and mirrors. Upgrade your testing equipment with this reliable and user-friendly instrument.
Packing List:
1*Manual Lensmeter
Technical Parameters:
Eyepiece focusing range: ±5 D
The vertex refraction measurement range: -20D ˜ +20 D
The minimum measurement grid: 0.12D
The prism measuring range: 5Δ
The prism grid value: 1Δ
The prism axis range: 1--180º
Prism grid value: 1º
Measuring the maximum diameter of the lens: 20mm-85mm
The exchange: 220V / 110V - 6V, DC:3V
Net Weight:
5KG
FDA Disclaimer:
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.Nancy-China-Beijing-86-15140779357
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.
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
Ultrasound ,Ultrasonic Treatment Device is certified with the US FDA 510(k) Number:K161892
This item has been cleaned and treated according to the manufacturer's instructions.