Specification:

Type: Scar Sheets

Size: 1.6”x 120”/4cm*300cm

 

 Instructions:

1. Use it after the wound has healed (or three to five days after the stitches are removed), and clean the scar before use;

 2. Cut a suitable size of scar sticker according to the size and shape of the scar. The area of the cut scar sticker should exceed the scar edge by about 1-2cm/0.4”-0.8”. Tear the inner package and stick the adhesive layer on the scar. Try to ensure that the scar is applied to the gel layer of the scar sticker.

 3. In order to adapt to the skin, apply 4-8 hours a day for the first few days, and then gradually increase to 24 hours a day.

 4. When taking it off, don't pull it at will, pull the two sides to the middle, and then gently open it.

 5. After removing the scar sticker, the wound needs to be ventilated for 1-2 hours before use, and the wound should be cleaned before use.

6. The product can be reused. If the product is soiled, it can be rinsed with water, dried or dried with a hair dryer before use. When the product is not in use, stick the release film on the gel surface of the product or put the product back in the packaging and store it in a cool, dry and clean place.

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 the manufacturer's instructions.Crystal-China-Beijing-86-15140779313


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