Portable Handheld Lensmeter Optometry Focimeter Eye Care Machine CE Certified

Description

Description:
This high Lensmeter/Focimeter is a must-have tool for glasses manufacturers, shops, and ophthalmologists. With the ability to test lens, prism refraction, cylindrical axis, prism baseline direction, optical center, cylinder axis, and cylinder base direction, this instrument ensures accurate measurements every time. The AC/DC dual power option makes it versatile and easy to use, while the clear scale readings provide intuitive results. The inclusion of a compensating prism allows for correction of center spot, making it ideal for measuring lenses and mirrors. Trust this reliable and user-friendly instrument for all your optical measurement needs.
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 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 manufacturer's instructions.
The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Europe 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