NON-TOUCH
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Sterile personnel must unscrew the container cap [8] and carefully drop the non-touch in the sterile field. STEP 3 The surgeon must pick up the non-touch from the sterile field and remove the cap [7] in the vertical position as shown in the figure. CAUTION: Opening the container in any other position (i.e., not vertical) and/or exerting excessive pressure upon the cap can cause the implant to accidentally fall outside the non-touch. STEP 4 A · Insertion of the implant using a wrench adapter. Remove the implant from the non-touch with the help of the wrench adapter: A1 · Index the hexagon of the adapter with the hexagon of the implant. A2 · Apply gentle pressure to adjust the fit between the implant and adapter to allow transport of the implant from the non-touch to the oral cavity. WARNING: To facilitate indexing between the implant and adapter, it is advisable to rotate the non-touch slightly. B · Implant insertion with wrench adapter. Remove the implant from the non-touch with the help of the wrench adapter: B1 · Index the hexagon of the wrench adapter with the hexagon of the implant. B2 · Apply gentle pressure to adjust the fit between the implant and adapter to allow transport of the implant from the non-touch to the oral cavity. WARNING: To facilitate indexing between the implant and adapter, it is advisable to rotate the nontouch slightly. CAUTION: Do not turn on the motor until the implant has been completely removed from the nontouch. NV VEGA IMPLANT NV VEGA IMPLANT NV VEGA IMPLANT NV VEGA IMPLANT RV VEGA IMPLANT RV VEGA IMPLANT RV VEGA IMPLANT RV VEGA IMPLANT Non-sterile personnel must open the sterile blister [1] and release the non-touch and identifying labels in the sterile field. MV VEGA IMPLANT MV VEGA IMPLANT MV VEGA IMPLANT MV VEGA IMPLANT RV VEGA IMPLANT RV VEGA IMPLANT RV VEGA IMPLANT RV VEGA IMPLANT STEP 5 Place the implant in the surgical bed and start insertion with the wrench adapter or motor. STEP 2.2 All KLOCKNER® IMPLANT SYSTEM products comply with the laws and regulations applicable to medical devices, such as: European directives MDD 93/42/ECC modified by 2007/47EC · Regulations of the United States FDA 21CFR 820 · Quality standards EN ISO 13485 and other applicable standards and regulations. Only for USA: SOADCO S. L. is a manufacturer of surgical-medical material, specifically dental implants and related surgical-medical products. KLOCKNER of North America, inc is the official distributor in USA. SOADCO S. L., KLOCKNER of North America and/or other official distributors do not practice medicine or dentistry and therefore do not recommend either surgical techniques or dental-medical equipment for patients. SOADCO S. L, KLOCKNER of North America, inc. and/or other official distributors do not guarantee a particular result or benefits arising from the use of such dental-medical equipment manufactured and/or sold by themselves, and decline / refuse any responsibility regarding the use of the material based on the interpretation of the information described in this document, because a particular outcome cannot be guaranteed. Any witness, opinion or instruction described in this document and distributed to any healthcare professional, clinician, researcher, or any qualified personnel are only their testimony, opinions, or instructions. These are not testimony, opinions, or instructions from employees of SOADCO S. L., KLOCKNER of North America, inc. and/or other official distributors. STEP 5 · WRENCH ADAPTER WARNING The material must be perfectly packaged upon receipt. If this is not the case, please contact your official distributor. Do not use if the packaging has been opened, is damaged or has expired. No sterile or single-use material should ever be reused under any circumstances, since the optimum conditions of quality and sterility with which the product is supplied would be lost, as would its performance. Therefore, SOADCO S. L., KLOCKNER of North America, inc. and/or other official distributors are not responsible for any claim or statement made by such parties. The products described in this document are for their acquisition and use only by dental-medical professionals appropriately trained and qualified in this field and must not be resold. The devices described in this document are manufactured by: SOADCO S. L, Avgda. Fiter i Rossell, 4 bis local nº 2 escaldes-engordany [Andorra] and distributed in usa by KLOCKNER of North America, inc. 175 sw 7 street, units 1103-1104 Miami Fl 33130 [USA] The use and/or selection of an inappropriate treatment of any medical and/or surgical materials described in this document, is solely responsibility of the user of such material. WARNING NOT ALL KLOCKNER® IMPLANTS SYSTEM PRODUCTS ARE AVAILABLE IN EVERY COUNTRY

PLATFORM SWITCHING The crestal area has been designed to achieve biological sealing according to the platform switching principle, generating optimum biological sealing to prevent bone reabsorption caused by bacterial infiltration through the connection gap. The platform switching dimensions for the different implants are: · Facilitation of clinical handling and correct positioning of the prosthetic components thanks to its good tactile sensation. · Optimization of the precision of fit between the hexagon of the internal connection of the implant and the hexagon of the abutments. ·...