-40%
Manual Lensmeter Optical Lensometer Focimeter Optometry Machine Reading Prism
$ 147.31
- Description
- Size Guide
Description
Description:This optical lensometer and focimeter is essential for testing lenses, prisms, cylindrical axes, and more. It provides accurate readings with clear scales for easy interpretation. The instrument is versatile with AC/DC dual power options and features a compensating prism for correcting measurements. Ideal for glasses manufacturers, shops, and ophthalmologists, this high instrument is reliable, user-friendly, and perfect for measuring lenses and mirrors.
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.(CICI-China-86-18328503374)
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.
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