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Product Description
Angular Standard M2 Multi Unit Set
The Angular Standard M2 Multi Unit Set is a comprehensive prosthetic solution designed for screw-retained full-arch and multiple-unit implant restorations where implant angulation correction is required. The system incorporates a titanium angular adapter available in 17° or 30° configurations, allowing clinicians and dental technicians to optimize the restorative path of insertion and improve prosthetic alignment.
Manufactured from medical-grade titanium alloys, the components provide excellent mechanical strength, precision fit, and long-term bio-compatibility. The set includes all essential prosthetic and laboratory components required for impression taking, model fabrication, restoration processing, and final prosthetic delivery.
The Angular Standard M2 Multi Unit Set is designed to facilitate predictable restorative workflows while compensating for implant angulations commonly encountered in full-arch and complex implant-supported rehabilitations.
Advantages
- Available with 17° or 30° angular correction options.
- Supports screw-retained full-arch and multiple-unit restorations.
- Improves prosthetic alignment and restorative access.
- Manufactured from high-quality medical-grade titanium.
- Precision-machined components ensure accurate fit and stability.
- Complete restorative and laboratory solution in one set.
- Compatible with conventional and digital restorative workflows.
- Facilitates predictable impression and prosthetic procedures.
- Designed for long-term clinical performance.
- Suitable for complex implant rehabilitation cases.
Components Included
- Titanium Angular Adapter – 17° or 30°
- Titanium Standard Connector for Angular Adapter 2 mm (630244) or 4 mm (630444)
- Fixation Screw (700229)
- Closed Screw Transfer for Connector Abutment (900929)
- Titanium Sheath for Titanium Standard Screw Abutment (687031)
- Plastic Sheath for Titanium Standard Screw Abutment (687030)
- Titanium Standard Connector Abutment Analog (920040)
- Long Fixation Screw for Transfer (711729)
Indications
- Screw-retained implant-supported restorations.
- Full-arch restorations on multiple implants.
- Multiple-unit prosthetic rehabilitations.
- Correction of implant angulation discrepancies.
- Fixed implant-supported prostheses.
- Laboratory and clinical restorative procedures involving angled multi-unit components.
Material
- Titanium components manufactured from medical-grade titanium alloys.
- Precision-engineered prosthetic and laboratory components.
Sterilization
- Components are supplied non-sterile unless otherwise specified.
- Before clinical use, all applicable components must be cleaned and sterilized according to validated clinical protocols.
- Steam sterilization in an autoclave at 135°C (274°F) is recommended prior to use.
Storage
Store in a clean, dry environment in the original packaging. Protect from contamination, excessive heat, moisture, direct sunlight, and mechanical damage.
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Angular Standard M2 Multi Unit Set
Intended Use
The Angular Standard M2 Multi Unit Set is intended for use in screw-retained implant-supported restorations where correction of implant angulation is required. The system is designed to support full-arch and multiple-unit prosthetic rehabilitations by providing a common restorative platform and facilitating prosthetic alignment.
Contraindications
Do not use:
- With implant systems not listed as compatible by the manufacturer.
- If any component is damaged, deformed, worn, or contaminated.
- In patients with conditions that contraindicate implant treatment.
- When implant stability or osseointegration is inadequate.
- If compatibility between components cannot be verified.
Warnings
- This product is intended for use only by qualified dental professionals and dental technicians.
- Use only original compatible components supplied by the manufacturer.
- Improper seating of components may result in screw loosening, prosthetic complications, or restoration failure.
- Do not modify implant connection surfaces or prosthetic interfaces.
- All components must be inspected prior to use.
Precautions
- Verify compatibility of all components before use.
- Ensure complete seating of the angular adapter and connector.
- Maintain proper torque values according to the implant system protocol.
- Avoid excessive occlusal loading during provisional and definitive restoration phases.
- Inspect all components for wear or damage before placement.
- Maintain traceability of product lot numbers in patient records.
Instructions for Use
Clinical Procedure
1. Verify implant integration and suitability for prosthetic restoration.
2. Select the appropriate Titanium Angular Adapter (17° or 30°) according to the clinical situation and restorative requirements.
3. Seat the angular adapter onto the implant and verify complete seating.
4. Secure the adapter using the Fixation Screw (700229) according to the recommended clinical protocol.
5. Select and connect the appropriate Titanium Standard Connector: 2 mm (630244), or 4 mm (630444)
6. Verify alignment, angulation correction, and prosthetic space.
7. Tighten the connector according to the manufacturer's recommended procedure.
Impression Procedure
1. Attach the Closed Screw Transfer for Connector Abutment (900929) to the connector.
2. Secure the transfer using the Long Fixation Screw for Transfer (711729).
3. Verify complete seating of the transfer.
4. Take the impression according to standard closed-tray impression techniques.
5. Remove the impression and transfer components according to accepted prosthetic protocols.
Laboratory Procedure
1. Connect the Titanium Standard Connector Abutment Analog (920040) to the transfer within the impression.
2. Fabricate the master model according to standard laboratory procedures.
3. Use the Titanium Sheath (687031) or Plastic Sheath (687030) as required for prosthetic fabrication.
4. Fabricate the screw-retained restoration according to accepted laboratory protocols.
5. Verify fit, passive adaptation, and structural integrity before delivery.
Final Restoration Placement
1. Verify passive fit of the definitive restoration.
2. Seat the restoration onto the connectors.
3. Tighten prosthetic screws according to the implant system protocol.
4. Verify occlusion, stability, and esthetics.
5. Seal screw access channels using accepted restorative materials.
6. Schedule routine follow-up examinations and maintenance visits.
Sterilization
- Components are supplied non-sterile unless otherwise specified.
- Clean and sterilize all applicable components using a validated steam sterilization cycle.
- Autoclave sterilization at 135°C (274°F) is recommended.
- Do not use components 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.
