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Hexagonal titanium screwdriver 1.2 millimeters - Titamed (IT0129) - Delynov

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The Tournevis hexagonal en titane 1,2 millimètres - Titamed is a medical device manufactured by Titamed BVClass I, CE marking CE0482.

  • Compliance: Medical device Class I, CE marking CE0482.
  • Manufacturer: Titamed BV.
  • Reference: IT0129.
  • Reserved for healthcare professionals. Read instructions carefully before use.

251.79 € 251.79 EUR 251.79 € Tax Included 344.95 €

251.79 € Tax Included 344.95 €

(0.00 € / Units)
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Instrument

What is the Titamed 1.2 millimeter titanium hexagonal screwdriver?

The 1.2 millimeter titanium hexagonal screwdriver, referenced under code IT0129 by the manufacturer Titamed, is a specialized manual instrument for bone surgery. Designed in titanium, this device combines lightness and strength to meet operating room requirements. Its structure is specifically adapted to fit into 1.2 millimeter hexagonal sockets. This implantology titanium screwdriver is a precision tool intended to facilitate technical manipulations during the assembly or fixation of bone stabilization devices within specialized surgeries.

What are the clinical indications for this 1 2 hexagonal screwdriver?

This 1 2 hexagonal screwdriver is specifically indicated for craniofacial and maxillofacial surgery interventions. Its use is intended for the manipulation of fixation elements requiring a 1.2 millimeter hexagonal socket. In clinical practice, it is used during the placement or removal phases of compatible osteosynthesis material or prosthetic components. This medical device from the Titamed brand is strictly reserved for use by qualified healthcare professionals, thus ensuring application in accordance with rigorous oral and facial surgical protocols.

What are the technical characteristics of the IT0129 titanium hexagonal screwdriver?

The IT0129 titanium hexagonal screwdriver is distinguished by its titanium construction, a material of choice for surgical instrumentation. Its tip features a hexagonal geometry precisely calibrated to 1.2 millimeters to ensure optimal torque transfer without damaging the screw head. As a Titamed product, it benefits from a rigorous industrial design adapted to sterile environments. This titanium implant screwdriver is delivered as a non-sterile instrument that must follow standard cleaning and sterilization protocols before any use at the surgical site, in accordance with the Titamed BV manufacturer's instructions.

What are the contraindications for the use of this instrument?

According to information provided by the manufacturer Titamed BV, there are no specific medical contraindications listed for the intrinsic use of this instrument, other than those related to the cranio- and maxillofacial surgery procedures themselves. However, the use of this surgical hexagonal screwdriver is strictly reserved for trained healthcare professionals. A poor match between the socket size (1.2 millimeters) and the component to be manipulated could lead to technical failure. It is imperative to read the instructions for use carefully before any intervention to ensure material compatibility.

What are the precautions for use and maintenance for this screwdriver?

The 1.2 millimeter titanium hexagonal screwdriver is a reusable medical device that requires special attention. Before each use, the practitioner must check the integrity of the hexagonal tip to prevent any risk of slipping during tightening. As a Class I device, it must be processed according to validated decontamination and sterilization cycles for titanium instruments. It is essential to respect the warnings from the manufacturer Titamed BV regarding exclusive use by healthcare professionals. Compliance with maintenance protocols guarantees the longevity of the instrument and patient safety during cranio- and maxillofacial surgeries.

Who is the manufacturer and what standards are met by this device?

This medical device is manufactured by Titamed BV, located in Kontich, Belgium. The 1.2 millimeter titanium hexagonal screwdriver (IT0129) complies with current European regulations, classified as a Class I device. It bears the CE0482 marking, attesting to its compliance with safety and performance requirements. The manufacturer Titamed requires a careful reading of the instructions to ensure optimal intended use. As a recognized supplier in the field of maxillofacial surgery, Titamed ensures the traceability and quality of its instruments intended for health experts.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

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Manufacturer Titamed
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