Titanium Base 1.5 For Implant Internal Hex H2.43

Titanium Base 1.5 for Implant Internal Hex H2.43

Intended Use

The Titanium Base 1.5 for Implant Internal Hex H2.43 provides an interface between a compatible dental implant and a custom prosthetic restoration, within the manufacturer’s approved indications.

For use by qualified dental professionals and trained dental laboratory personnel.

Compatibility & Selection

- Confirm compatibility with the exact implant model and prosthetic platform.
- Use only the fixation screw and driver specified for this titanium base.
- For digital fabrication, select the corresponding validated CAD/CAM library.
- Confirm that the engaging hexagonal design is approved for the planned restoration.
- The H2.43 designation alone does not establish compatibility with every internal hex implant system.

Preparation Before Use

- Check the product identification and packaging.
- Inspect the base and screw for damage, deformation, contamination, or defects.
- Do not use components with damaged connection surfaces, screw seats, or threads.
- Check the product label for its sterile or non-sterile status.
- Follow the manufacturer’s validated processing instructions before clinical use.

Laboratory Procedure

- Verify complete seating and rotational engagement on the compatible implant analog.
- Design the restoration within the approved dimensions, material requirements, and restorative indications.
- Modify the titanium base only where expressly permitted by the manufacturer. Do not alter the implant connection, screw seat, or screw channel.
- Where bonding is indicated, follow the approved surface-treatment and bonding instructions for the base, restorative material, and bonding agent.
- Protect the connection surfaces and screw channel from abrasive particles and bonding material.
- Remove excess bonding material and inspect the completed restoration for fit and unobstructed screw access.
- Process the completed restoration according to validated instructions before clinical placement.

Clinical Placement

- Inspect and clean the implant interface according to the implant system instructions.
- Position the restoration, aligning the hexagonal connection with the implant.
- Verify complete seating without force. Do not use screw tightening to pull an incompletely seated restoration into position.
- Insert the specified fixation screw using the correct driver.
- Tighten with a calibrated torque instrument to the manufacturer’s prescribed torque for the exact implant, base, and screw combination.
- Verify seating, stability, proximal contacts, and occlusion. Perform radiographic assessment when clinically indicated.
- Complete screw-access closure according to the approved restorative protocol.

Cleaning & Sterilization

Follow the manufacturer’s validated instructions for cleaning, disinfection, packaging, sterilization, and drying.

The prescribed sterilization procedure must include the cycle type, temperature, exposure time, and drying requirements. Confirm that processing is suitable for the completed restoration and its bonding materials.

A sterilization temperature alone is not a complete processing protocol.

Warnings & Precautions

- Secure small components against accidental swallowing or aspiration.
- Do not exceed the specified tightening torque.
- Do not combine components with unverified compatibility.
- Do not use in patients with known hypersensitivity to the component’s materials.
- Follow the product labeling concerning single use and reuse restrictions.
- Resolve any seating, fit, or fixation problems before completing treatment.