Helical Drill Bit, Ø 1.0 mm, Length=50 mm, Stop 5 mm Dental Drill - Titamed (IT105005) - Delynov

What is the Titamed IT105005 twist drill?

The Titamed IT105005 twist drill is a high-precision rotary instrument specifically developed for bone surgery procedures. This implantology drill is distinguished by a helical design optimized for the evacuation of bone debris during drilling. Manufactured by Titamed BV, this drill has a diameter of 1.0 mm and a total length of 50 mm. Its structure integrates a fixed stop located 5 mm from the active tip, providing an essential physical reference for the practitioner during site preparation. This instrument is a technical component used to create precise drill holes in bone tissue before the placement of implants or osteosynthesis devices.

What are the clinical indications for this osteosynthesis drill?

This osteosynthesis drill is indicated for the preparation of screwing or implantation sites in oral and maxillofacial surgery. Its use is common in osteosynthesis plate fixation protocols where a 1.0 mm pre-hole is required. In implantology, this surgical twist drill can be used for initial marking or the creation of a small-diameter guide tunnel. The presence of a 5 mm stop limits the insertion of the instrument, which is particularly useful in areas with low bone volume or near sensitive anatomical structures. It allows for a standardized and secure approach during cortical and cancellous drilling phases.

What are the technical characteristics of the IT105005 drill?

The Titamed IT105005 twist drill presents rigorous technical specifications to meet the requirements of modern implantology. It has a cutting diameter of 1.0 mm, ideal for precision work. Its 50 mm length allows for easy use with standard surgical contra-angles, providing satisfactory visibility of the operative field. The major feature of this model is its 5 mm fixed depth stop, which prevents any progression beyond this measurement. This technical configuration guarantees repeatability of the surgical gesture and strict management of the drilling depth, thus reducing the risks of manual measurement error during the intervention.

What are the contraindications for the use of this instrument?

Contraindications for the use of the Titamed twist drill mainly concern clinical situations where bone density is insufficient to guarantee instrument stability or when the available space is less than the length of the stop (5 mm). Use is also prohibited in cases of known hypersensitivity to the metallic components of the instrument, although the specific material is not detailed here. It is imperative not to use this drill if the equipment shows signs of wear, deformation, or loss of sharpness, as this could lead to excessive thermal heating of the bone (bone necrosis). The practitioner must evaluate the quality of the bone stock by imaging before any use.

What are the maintenance and durability precautions?

As a surgical cutting instrument, the Titamed twist drill requires rigorous maintenance to maintain its performance. Although resorption details do not apply to this non-implantable instrument, the management of its life cycle is crucial. The practitioner must ensure the systematic cleaning of the helical flutes to eliminate biological residues after each use. Appropriate lubrication of the connection area to the drill or contra-angle is recommended. It is essential to regularly check the sharpness of the drill; a blunt drill requires stronger axial pressure, increasing the risk of deviation or thermal injury to surrounding tissues. Compliance with the sterilization protocols of the manufacturer Titamed BV is mandatory.

Who is the manufacturer and what standards are respected?

The device is manufactured by Titamed BV, a company specializing in the design of solutions for osteosynthesis and maxillofacial surgery. The Titamed brand is recognized for the precision of its rotary instruments. Regarding regulatory certifications such as the device class or specific CE marking, this information is not specified in the current technical documentation. It is the responsibility of the healthcare professional to consult the instructions for use provided with the IT105005 product and to check the regulatory labeling affixed to the packaging before any intervention. The product must be used in accordance with good surgical practices and current recommendations for rotary medical devices.

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