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Product Description
Titanium Abutment for Conical Implant CH2.1
The Titanium Abutment for Conical Implant CH2.1 is a precision-engineered prosthetic component designed for cement-retained implant-supported restorations. Manufactured from medical-grade Ti6Al4V ASTM F136 titanium alloy, this abutment provides excellent strength, bio-compatibility, and long-term clinical reliability.
Featuring a straight profile with an anti-rotational cone and 2.1 mm hex connection, the abutment ensures precise positioning and a secure implant-abutment interface. The conical connection design promotes stability and accurate restoration seating while supporting predictable prosthetic outcomes.
The abutment connects directly to compatible CH2.1 implants using fixation screw 701203 UNF 1-72 and is intended for use in single-unit and multiple-unit cement-retained restorations. Its optimized dimensions provide a reliable foundation for prosthetic fabrication while maintaining restorative flexibility.
Advantages
- Manufactured from medical-grade Ti6Al4V ASTM F136 titanium alloy.
- Conical implant-abutment connection for enhanced stability and precision.
- Anti-rotational cone and 2.1 mm hex design for accurate positioning.
- Designed for cement-retained implant restorations.
- Excellent mechanical strength and corrosion resistance.
- Bio-compatible material suitable for long-term clinical use.
- Direct connection to CH2.1 implant platform.
- Compatible with multiple UMI and PMI implant diameters.
- Supports predictable prosthetic outcomes and restoration stability.
Specifications
- Connection: CH2.1 Cone + Hex 2.1 mm
- Diameter: 3.9 mm
- Height: 9 mm
- Material: Ti6Al4V ASTM F136 Titanium Alloy
- Fixation Screw: 701203 UNF 1-72
Compatible Implants
- UMI Implants Diameters: Ø3.3 mm, Ø3.75 mm
- PMI Implants Diameters: Ø3.3 mm, Ø3.75 mm, Ø4.2 mm
Indications
- Cement-retained implant-supported restorations.
- Single-unit and multiple-unit prosthetic restorations.
- Implant prosthetic rehabilitation on compatible CH2.1 implant platforms.
Sterilization
The product is supplied non-sterile. Prior to clinical use, sterilization in an autoclave at 135°C (274°F) is required according to validated sterilization procedures.
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Titanium Abutment for Conical Implant CH2.1
Intended Use
The Titanium Abutment for Conical Implant CH2.1 is intended for use with compatible dental implants to support cement-retained implant-supported restorations.
Contraindications
Do not use:
- With implant systems not listed in these instructions.
- If the component is damaged, deformed, or contaminated.
- In patients with conditions that contraindicate implant treatment.
- When compatibility with the implant system cannot be verified.
Warnings
- This product is intended for use only by qualified dental professionals.
- Use only original compatible components and fixation screws.
- Failure to properly seat the abutment may result in mechanical complications, component loosening, or restoration failure.
- Improper prosthetic procedures may compromise the fit, function, and longevity of the restoration.
Precautions
- Verify implant compatibility before use.
- Inspect the abutment and fixation screw prior to use.
- Confirm complete seating of the abutment before tightening the fixation screw.
- Verify proper fit clinically and radiographically.
- Follow accepted clinical protocols for implant restoration and maintenance.
- Maintain traceability of the product lot number in patient records.
Instructions for Use
Clinical Procedure
1. Verify compatibility of the abutment with the selected implant system.
2. Remove the healing component or cover screw and clean the implant connection.
3. Seat the Titanium Abutment for Conical Implant CH2.1 into the implant connection and verify complete seating.
4. Secure the abutment using fixation screw 701203 UNF 1-72 and tighten according to the implant system protocol.
5. Verify the position and fit of the abutment clinically and radiographically.
6. Fabricate or place the definitive restoration as indicated.
7. Verify occlusion, stability, and soft tissue adaptation.
8. For cement-retained restorations, remove all excess cement.
9. Perform routine follow-up examinations according to accepted clinical protocols.
Sterilization
- The product is supplied non-sterile.
- Before clinical use, clean and sterilize the abutment using a validated steam sterilization cycle. Autoclave sterilization at 135°C (274°F) is required prior to placement.
- Do not use the product if sterility cannot be assured.
Storage
Store in a clean, dry environment in the original packaging. Protect from contamination, excessive heat, direct sunlight, moisture, and mechanical damage.
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