Product Description

The Hahn^™ Tapered Implant Guided Shaping Drill for Dense Bone is designed for guided dental implant surgery in dense bone types. The drill is stepped to accommodate the tapered shape of the implant.

• Machined from corrosion-resistant, surgical stainless steel
• Features standard ISO latch connectivity and a flange stop for depth control
• Designed to achieve maximum cutting efficiency while effectively removing bone from the osteotomy
• Diameter- and length-specific

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.

Do NOT use any drill that exceeds the diameter or length of the prescribed implant.

Hahn Tapered Implant Guided Shaping Drills for Dense Bone should NOT be used in soft bone types (Type III, Type IV).

Sterility

Hahn Tapered Implant Guided Shaping Drills for Dense Bone 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 15 minutes at 132^°C (270^°F). Allow sterilized components to dry for at least 30 minutes.

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.

Technical Specifications

Diameter: 3.5 mm

Length: 8 mm

Connection Type: Standard ISO latch