The pick-up procedure is considered to be most precise method. For positioning the analogues in the working model. However, depending on the system used, the manufacture. Of an individual impression tray might be necessary. Additional time, costs and another appointment for the patient. Is an impression tray with removable segments-it is rigid. Re-usable and can be sterilized and only a single appointment is. Required for casting a perfect working model. Do not use adhesives! Select the size of impression tray and remove the appropriate. Segments for the posts in the dental arch from the impression. Load the impression tray with impression material and press it. Onto the dentition until the screws in the impression posts can be. Once the material has hardened, loosen the holding screws of. The impression posts and remove the impression tray from. The impression posts remains firmly positioned into the. Usually, the material can be removed easily from the impression. Tray without being cut. Single or multiple placement. The WINTRAY with removable segments can be used for taking impression of all. Of the dental arches, regardless of their shape, as it is available in several. The correct numbered segment for the clinical situation is removed to expose the. Placing implants in edentulous cases. When fabricating the -supported full dentures, several to all segments can. The impression tray is used in the same way. As the impression material is accessible, when fabricating tooth-bome restorations. The impression can be removed from the model without fracturing the slender. It is made of stainless steel and as a consequence sterilizable and fulfills therefore. All requirements in the traceability of the procedure of the sterilization. Clean the impression tray and the removed segments carefully by using customary. Strongly as the thread might overload and break. Take through the sterilization procedure in the normal waymax. The sale of this item may be subject to regulation by the U. Food and Drug Administration and state and local regulatory agencies. IMPORTANT INFORMATION ON OUR POLICY AND FEEDBACK. Feedback if you are satisfied with our items. We try to be fair and accurate with all of our product listings and descriptions. If there is a problem, we can work together to resolve it. We strive to always be extremely fair and always try to work with reasonable customers. We will always make every attempt possible to resolve issues if we made a mistake. Please do not assume a mistake is intentional. Let us know if our service could be better! Tracking info of your parcel is available. The following form is for your reference. Please repack the item carefully. FDA for Curing Light. 510(K) Number: K192233. Regulation Number: 21 CFR 872.6070. 510(K) Number: K181691. Regulation Number: 872.4200. Classification Product Code: EFB. Subsequent Product Code: EGS. 510(K) Number: K163414. Regulation Number: 872.4850.