Product Code: 70-1071-SRG0088
Handpiece Implant Driver
Prismatik Dentalcraft

Product Description

A Hahn Tapered Implant Driver is intended for use in the seating and rotation of dental implants. The driver can be used with a handpiece motor or in conjunction with the Surgical Adaptor and the Driver Handle, Ratchet Wrench, or Adjustable Torque Wrench.

  • Machined from corrosion-resistant, surgical stainless steel
  • Features standard ISO latch connectivity

Accessories

None

Contraindications

Patients should be evaluated before the time of surgery for factors that put them at risk from the implant placement procedure, or that may affect healing of bone or surrounding soft tissue. Contraindications include but are not limited to: vascular conditions, uncontrolled diabetes, clotting disorders, anticoagulant therapy, metabolic bone disease, chemotherapy or radiation therapy, chronic periodontal inflammation, insufficient soft tissue coverage, metabolic or systemic disorders associated with wound and/or bone healing, use of pharmaceuticals that inhibit or alter natural bone remodeling, any disorders which inhibit a patient's ability to maintain adequate daily oral hygiene, uncontrolled parafunctional habits, insufficient height and/or width of bone, and insufficient interarch space.

Sterility

Hahn Tapered Implant Drivers 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

Diameter: Ø7.0

Length: Short

Connection Type: Standard ISO latch / 4 mm hex

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