Description: Description: This eye care equipment, optometry device is a lens tester used to test the lens of the lens, prism refraction, cylindrical axis, and prism baseline direction. It can also print marks for the optical center of the lens, cylinder axis, and cylinder base direction. The instrument is powered by AC or DC (5 DC battery) for convenience. With clear and intuitive readings, high, good reliability, and simple operation, this tester is ideal for glasses manufacturers, shops, and ophthalmologists. It even includes a compensating prism to correct the center of the spot, making it a versatile measuring instrument for 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 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.（Seller name:Edela City:Beijing State:Beijing Country:China Phone:+86 18332651236） 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
Price: 278.95 USD
Location: Cranbury, New Jersey
End Time: 2024-09-11T16:13:00.000Z
Shipping Cost: 0 USD
Product Images
Item Specifics
Restocking Fee: No
Return shipping will be paid by: Buyer
All returns accepted: Returns Accepted
Item must be returned within: 30 Days
Refund will be given as: Money Back
Brand: Carejoy
MPN: Does Not Apply
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
