Description:
Instructions:
1.Remove one strip from the bottle and replace the cap immediately.
2.Immerse the reagent area of the strip in the urine specimen and take it out quickly.
3.Wipe off excess urine against the rim of the specimen container.
4.Read the test results carefully within 60s in a good light and with the test area held near the appropriate color chart on the bottle label.Changes in color that appear only along the edges of the test pads or after moving than 2min have passed are of no diagnostic significance.Results with leukocytes test portion can be read within 120s.
If reading instrumentally,carefully follow the directions given in the appropriate instrument operating manual.
Package Include:
100 strips/Bottle Ketone Test Strips
Note:
1.Due to the difference between different monitors, the picture may not reflect the actual color of the item. Thank you!
2.This product has a shelf life of two years and we will ship it according to the most recent production date.
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.
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.
Lucy-China-Beijing-86-18569215430