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Synthacer® / Syntricer® Bone Void Filler
Special Warning
Synthacer®/Syntricer® cannot assume any load-bearing functions. Additional stabilization using osteosynthetic measures may be needed depending on the type and lo- cation of the defect to be treated.
Interactions
No interactions between Synthacer® and pharmaceuti- cals or other medical devices have been reported to date excepot the direct in-contact combination with sti im- plants.
Single Use, Sterilization, Shelf life and Storage
Synthacer®/Syntricer® Cylinders Synthacer®/Syntricer® Blocks , Synthacer®/Syntricer® Wedges are packaged dou- ble sterile (Gamma irradiation). Implants are delivered in shockproof membrane-boxes.
Synthacer®/Syntricer® Ceraball® and Synthacer®/Syntricer® Granules, as well as Synthacer®/Syntricer® Ceround® are packaged double sterile in small ampoules ready for ap- plication.
Synthacer®/Syntricer® products are intended for single use only; re-sterilization is not allowed.
Synthacer®/Syntricer® products are packaged shockproof and should only be removed from the box immediately before use; the package provides damping properties and protects the implant.
Mechanical damage can infringe the strength of the material; therefore attention has to be paid to open the membrane-box or the ampoule only shortly before use.
e product must not be used if the sterile packaging shows visible signs of damage. Before use, the intactness of the packaging has to be checked.
e medical device must be stored dry in its transport box.
Synthacer®/Syntricer® products must not be used af- ter the expiration date. Unused and unopened expired products can be disposed as household waste. Discarded (used and unused) devices are classi ed as healthcare (clinical) waste and have to be disposed.
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