Product Description

Hahn Tapered Implant Non-Engaging Temporary Abutments are indicated for the fabrication of temporary screw-retained restorations. Provisional restorations can be made chairside using any standard fabrication technique (e.g., vacuum-formed sheet, prefabricated crown/bridge form, etc.). Temporary abutments are precisely machined from titanium alloy and attached to the implant fixture (or implant analog) by a titanium screw or provisional guide pin. Each temporary abutment is specific to the restorative platform of the seated implant.

• Precisely machined from titanium alloy
• These non-engaging temporary abutments are indicated for multi-unit bridges, and therefore avoid the unnecessary anti-rotational implant connection feature to allow for a passive path of insertion.

Accessories

Each Hahn Tapered Implant Non-Engaging Temporary Abutment is packaged with a separate provisional screw (Hahn Tapered Implant Guide Pin) and separate retaining screw (Hahn Tapered Implant Titanium Screw) compatible with the restorative instrumentation of the specified implant system. The guide pin should be used throughout the fabrication process. The titanium screw should only be utilized to retain the finished provisional.

Sterility

Hahn Tapered Implant Non-Engaging Temporary Abutments are shipped NON-STERILE. Non-sterile items must be cleaned, disinfected, and sterilized prior to clinical use, according to a validated method.

• Cleaning: Wash using a broad spectrum cleaning solution, followed by thorough rinsing and drying.

The recommended disinfection process is based on ANSI/AAMI ST79 guidelines, as follows:

• Disinfection: Immerse abutments in disinfectant¹, rinse with distilled water and dry.

The recommended sterilization process is based on the ANSI/AAMI/ISO 17665-1 and ANSI/AAMI ST79 guidelines, as follows:

• Sterilization: Gravity-fed sterilizers: Autoclave in sterilization pouch for 30 minutes at 121°C (250°F)². Devices are to be used immediately after sterilization.

NOTE: The validated procedures require the use of FDA-cleared sterilization trays, wraps, biological indicators, chemical indicators, and other sterilization accessories labeled for the sterilization cycle recommended. The healthcare facility should monitor the sterilizer for the facility according to an FDA-recognized sterility assurance standard such as ANSI/AAMI ST79.

¹Oral disinfectant containing Chlorhexidine is recommended; refer to the disinfectant manufacturer's instructions. ²ANSI/AAMI ST79

Technical Specifications

Platform: Ø5.0

Material Composition: Titanium alloy (Ti6Al4V)