Titanium Base For Implant H2.1 - 1mm With Screw 1-72UNF

Titanium Base for Implant H2.1 – 1 mm with Screw 1-72 UNF

Intended Use

The Titanium Base for Implant H2.1 – 1 mm provides an interface between a compatible H2.1 implant and a custom prosthetic restoration. Use only for restoration types and clinical applications approved by the manufacturer for this specific component.

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

Compatibility & Component Selection

- Confirm the exact implant model, platform, and titanium base reference before use.
- Use the supplied 1-72 UNF fixation screw only with the components for which it is specified.
- Thread designation alone does not establish screw compatibility; screw length, head geometry, and seating surfaces must also match.
- For CAD/CAM fabrication, select the validated digital library corresponding to the exact titanium base.
- Confirm whether the base’s engaging or non-engaging design is suitable for the planned restoration.

Preparation Before Use

- Check product identification, packaging, and labeling.
- Inspect the base and screw for damage, deformation, or contamination.
- Do not use components with damaged threads, connection surfaces, or screw seats.
- Verify the sterile or non-sterile status on the label.
- Process the components according to the manufacturer’s validated instructions before clinical use.

Laboratory Procedure

- Verify complete seating on the specified implant analog.
- Design the restoration within the approved dimensional and material limits.
- Modify the base only where expressly permitted by the manufacturer. Preserve the implant connection, screw seat, and screw channel.
- Where bonding is indicated, follow the approved surface-treatment and bonding protocols for the titanium base, restorative material, and bonding agent.
- Protect the implant interface and screw channel from abrasive particles and bonding material.
- Remove excess bonding material and inspect the completed restoration.
- Follow the validated processing instructions for the completed restoration before clinical placement.

Clinical Placement

- Inspect and clean the implant interface according to the implant system instructions.
- Position the restoration and align any engaging connection features.
- Verify complete seating without force. Do not use the screw to pull an incompletely seated restoration into position.
- Insert the specified 1-72 UNF fixation screw using the correct driver.
- Tighten with a calibrated torque instrument to the manufacturer’s prescribed torque for this 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 complete procedure must specify the sterilization method, cycle type, temperature, exposure time, and drying requirements. Confirm that the selected procedure is suitable for the assembled restoration and any bonding materials.

Do not substitute a sterilization protocol from another component.

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 labeling concerning single use and reuse restrictions.
- Resolve any fit, seating, or fixation problems before completing treatment.