3M ESPE Filtek Z250 Mode D'emploi page 3

2.8 Place the die back into the articulated arch, add the last third of incisal
composite to the occlusal surface. Overfill very slightly mesially, distally, and
occlusally. This will allow for the mesiodistal contacts and the proper occlusal
contact when the opposing arch is brought into occlusion with the uncured
incisal increment. Light cure for only 10 seconds, then remove the die to prevent
adhering to adjacent surfaces. Finish the curing process.
2.9 With the occlusal contacts already established, begin removing the excess
composite from around the points of contact. Develop the inclines and ridges as
per remaining occlusal anatomy.
2.10 Care must be taken when removing the prosthesis from the die. Break off
small amounts of the die from around the restoration, the die stone should
breakaway cleanly from the cured restoration, until all of the restoration is
recovered.
2.11 Using the master die, check the restoration for flash, undercuts, and fit. Adjust
as necessary, then polish.
3. Dental Operatory Procedure
3.1 Roughen the interior surfaces of the indirect restoration.
3.2 Clean the prosthesis in a soap solution in an ultrasonic bath and rinse
thoroughly.
3.3 Cementation: Cement the prosthesis using a 3M ESPE resin cement system by
following manufacturer's instructions.
Storage and Use
This product is designed to be used at room temperature. If stored in cooler allow
product to reach room temperature prior to use. Shelf life at room temperature is 36
months. Ambient temperatures routinely higher than 27°C/80°F may reduce shelf life.
See outer package for expiration date.
Do not expose restorative materials to elevated temperatures, or to intense light.
Do not store materials in proximity to eugenol containing products.
Disinfect the products using an intermediate level disinfection process (liquid contact)
as recommended by the Centers for Disease Control and endorsed by the American
Dental Association, Guidelines for Infection Control in Dental Health-Care Settings,
2003. MMWR , December 19, 2003:52(RR-17), Centers for Disease Control and
Prevention.
Disposal – See the Material Safety Data Sheet (available at www.3MESPE.com or
through your local subsidiary) for disposal information.
Customer Information
No person is authorized to provide any information which deviates from the information
provided in this instruction sheet.
Caution: U.S. Federal Law restricts this device to sale or use on the order of a
dental professional.
Warranty
3M ESPE warrants this product will be free from defects in material and manufacture.
3M ESPE MAKES NO OTHER WARRANTIES INCLUDING ANY IMPLIED WARRANTY
OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. User is
responsible for determining the suitability of the product for user's application. If this
product is defective within the warranty period, your exclusive remedy and 3M ESPE's
sole obligation shall be repair or replacement of the 3M ESPE product.
Limitation of Liability
Except where prohibited by law, 3M ESPE will not be liable for any loss or damage
arising from this product, whether direct, indirect, special, incidental or consequential,
regardless of the theory asserted, including warranty, contract, negligence or strict
liability.
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