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Product Description
The Straight Titanium Abutment with Shoulder for Implant CH2.1 is a prefabricated prosthetic component designed for cement-retained implant restorations. Featuring a straight profile with an integrated prosthetic shoulder, this abutment provides a stable and precise foundation for the fabrication of implant-supported crowns and bridges while supporting optimal emergence profile development.
Manufactured from medical-grade Ti6Al4V titanium alloy in accordance with ASTM F136 standards, the abutment offers exceptional strength, bio-compatibility, and long-term clinical reliability. The component incorporates an anti-rotation connection featuring a cone and 2.1 mm hex interface, ensuring accurate positioning and stability during prosthetic treatment.
The abutment connects directly to the implant using titanium fixation screw 701203. With a shoulder diameter of 4.5 mm, it is designed to provide predictable prosthetic support and facilitate the fabrication of aesthetically pleasing cement-retained restorations.
Key Features
- Designed for cement-retained restorations
- Straight abutment design
- Integrated prosthetic shoulder
- Shoulder diameter: 4.5 mm
- Anti-rotation connection with cone and H2.1 mm hex
- Manufactured from Ti6Al4V ASTM F136 medical-grade titanium
- Direct implant connection using screw 701203
- High mechanical strength and biocompatibility
- Precision-machined implant interface
- Intended for professional dental use
Advantages
- Provides a stable foundation for cement-retained restorations
- Anti-rotation design enhances prosthetic stability and positioning accuracy
- Integrated shoulder supports optimal emergence profile development
- Precision implant connection promotes predictable restorative outcomes
- Manufactured from high-strength medical-grade titanium alloy
- Excellent biocompatibility and corrosion resistance
- Supports long-term clinical performance
- Simplifies restorative procedures through a prefabricated design
- Compatible with multiple implant diameters within the CH2.1 platform
- Suitable for single-unit and multi-unit restorative applications
Compatible Implant Systems
- UMI Implants Diameters: Ø3.3 mm, Ø3.75 mm
- PMI Implants Diameters: Ø3.3 mm, Ø3.75 mm, Ø4.2 mm
Sterilization
The product is supplied non-sterile.
Before clinical use, the abutment must be sterilized in a steam autoclave using a validated sterilization cycle.
Recommended sterilization temperature: 135°C (275°F)
Follow the autoclave manufacturer's instructions regarding exposure and drying times.
Applications
The Straight Titanium Abutment with Shoulder for Implant CH2.1 is used for the fabrication of cement-retained implant-supported restorations. It provides a precise and stable prosthetic platform for crowns and bridges while supporting functional performance, aesthetic outcomes, and long-term restorative success.
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Straight Titanium Abutment with Shoulder for Implant CH2.1
Intended Use
The Straight Titanium Abutment with Shoulder for Implant CH2.1 is intended for use as a prosthetic component in the fabrication of cement-retained implant-supported restorations.
Contraindications
Do not use:
- In patients with known hypersensitivity or allergy to titanium alloys.
- With implant systems not listed in these instructions.
- If the component is damaged, deformed, or contaminated.
- If proper implant stability has not been achieved.
Warnings
- This product is intended for use only by qualified dental professionals.
- Use only original compatible components and fixation screws.
- Improper placement or restoration design may result in prosthetic complications or component failure.
- Ensure complete seating of the abutment before tightening the fixation screw.
- Do not modify the implant connection geometry.
Precautions
- Verify implant compatibility before use.
- Inspect the abutment and fixation screw prior to use.
- Follow accepted prosthetic and restorative procedures.
- Maintain traceability of the product lot number in patient records.
- Ensure proper oral hygiene and routine maintenance following restoration placement.
Instructions for Use
Clinical Procedure
1. Verify compatibility of the abutment with the implant system.
2. Inspect the abutment and fixation screw for damage or contamination.
3. Sterilize the components before clinical use.
4. Seat the abutment onto the implant, ensuring proper engagement of the cone and hex connection.
5. Insert fixation screw 701203 and tighten according to the implant system's recommended torque value.
6. Verify complete seating and stability of the abutment.
7. Fabricate or place the cement-retained restoration.
8. Remove all excess cement after restoration placement.
9. Verify occlusion, restoration fit, and soft tissue adaptation.
Sterilization
- The product is supplied non-sterile.
- Before clinical use, sterilize the abutment in a steam autoclave using a validated sterilization cycle.
- Recommended sterilization temperature: 135°C (275°F)
Follow the autoclave manufacturer's instructions regarding exposure and drying times.
Storage
Store in a clean, dry environment in the original packaging. Protect from contamination, moisture, and mechanical damage.
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