Product Code: 70-1153-PRA0030
Scanning Abutment
Prismatik Dentalcraft

Product Description

Hahn Tapered Implant Clinical Scanning Abutments, Posterior are used to transmit highly accurate position and angulation data of seated implants when scanned with an intraoral scanner. Each scanning abutment is specific to the restorative platform of the seated implant and consists of an abutment body manufactured from biocompatible PEEK material. Retained within the abutment body by internal threading is a screw manufactured from titanium alloy. Always use the internal screw to attach the scanning abutment to the implant, tightening the screw to hold the scanning abutment in place.

  • Contains a radiopaque, barium-sulfate material designed for chairside use with intraoral scanners
  • When connected to the original implant body, its opacity on a radiograph allows accurate confirmation of complete seating
  • Designed to accommodate ease of attachment in the posterior arch

Accessories

Each Hahn Tapered Implant Clinical Scanning Abutment, Posterior is packaged with a captured screw.

Contraindications

Hahn Tapered Implant Clinical Scanning Abutments should not be used for elastomeric impressions or bite registrations. Placed intraorally (attached to an implant in a patient's mouth), Hahn Tapered Implant Clinical Scanning Abutments are intended for single use only. Multiple use in a clinical setting is contraindicated due to potential scan inaccuracies and the risk of cross-contamination.

Sterility

Hahn Tapered Implant Clinical Scanning 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: Ø3.0

Material Composition: Polyether ether ketone (PEEK), Titanium alloy (Ti6Al4V)

Just added to your wishlist:
My Wishlist
You've just added this product to the cart:
Go to cart page