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Lindemann bone cutter C254 for XXL turbine - Ø 1.2 mm L 6 mm - JOTA - Delynov - [C254.FGXXL.012]

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The Fraises Lindemann bone cutter C254 pour turbine XXL - Ø 1,2 mm L 6 mm - JOTA is a medical device manufactured by le fabricantClass IIa, CE marking CE0483.

  • Compliance: Medical device Class IIa, CE marking CE0483.
  • Manufacturer: le fabricant.
  • Reserved for healthcare professionals. Read instructions carefully before use.

65.31 € 65.31 EUR 65.31 € Tax Included 93.58 €

65.31 € Tax Included 93.58 €

(0.00 € / Units)
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What is the Lindemann C254 bur for XXL turbine?

The Lindemann bone cutter C254 from JOTA is a rotary cutting instrument specifically developed for bone surgery. This XXL model features a diameter of 1.2 mm and a working length of 6 mm. Designed to be mounted on a turbine, this xxl surgical bur is manufactured from high-quality metallic or plastic materials, ensuring cutting performance adapted to clinical requirements. As a device in the CONSO category, it is delivered non-sterile and requires a complete cleaning and sterilization protocol before its first use in the office or operating room.

What are the clinical indications for this surgical bur?

This lindemann fg bur is indicated for oral and implant surgery interventions requiring a clean section of hard tissues. Its primary use concerns osteotomy, root separation, or bone remodeling. Thanks to its turbine configuration, it allows for high rotation speeds essential for certain cutting techniques. The manufacturer JOTA AG specifies that these instruments are classified as semi-critical. The practitioner must ensure that the bur is free from any contamination before the procedure, following validated reprocessing procedures to maintain patient safety during invasive surgeries.

What are the technical characteristics of reference C254.FGXXL.012?

The technical reference C254.FGXXL.012 from JOTA is distinguished by its precise dimensions: a cutting diameter of 1.2 mm and an active part 6 mm long. Its shank is adapted for turbine-type (FG) chucks. This medical device belongs to Class IIa and bears the CE0483 marking, certifying its compliance with European regulatory requirements. The structure of the lindemann turbine bur is optimized to minimize thermal heating while maximizing bone removal efficiency. It is compatible with ultrasonic cleaning agents, provided they do not form foam and respect the material resistance of the instrument.

What are the contraindications for the use of this instrument?

There are no absolute contraindications listed other than manifest wear of the product. According to the recommendations of the manufacturer JOTA AG, the use of a blunt, deformed instrument or one showing signs of breakage constitutes a major contraindication as it compromises safety and leads to failing performance of the device. The user physician is solely responsible for evaluating the condition of the turbine surgical bur before each intervention. In case of doubt regarding structural integrity or if specific labeling mentions contrary restrictions, it is imperative to replace the instrument with a new one to avoid any intraoperative risk.

What are the maintenance and reuse precautions?

The turbine bone surgery bur from JOTA is reusable subject to rigorous reprocessing. The protocol includes cleaning and disinfection (manual or in a washer-disinfector) followed by steam sterilization. It is crucial to use sterile demineralized or low-contamination water (max. 10 germs/ml) and low in endotoxins for the final phases. The practitioner must respect the concentrations, temperatures, and soaking times recommended by the detergent manufacturers. Particular attention must be paid to the compatibility of chemical agents to avoid corrosion. Sterilization must be performed after packaging to ensure the maintenance of the sterile state until use.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is JOTA AG, located in Rüthi, Switzerland. This product is a Class IIa medical device, bearing the CE0483 marking. The manufacturer guarantees compliance with European safety standards for surgical rotary instruments. All reprocessing instructions provided by JOTA AG apply to their entire range distributed by Delynov. The responsibility for final sterility lies with the user, who must implement validated procedures and ensure that sterilization devices are regularly monitored and maintained according to approved parameters.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer JOTA Professional Rotary Instruments
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