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Periotome #1, posterior, Black Line

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The Periotome #1, postérieur, Black Line is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.

  • Compliance: Medical device Class I.
  • Manufacturer: Hu-Friedy Mfg. Co., LLC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

88.65 € 88.65 EUR 88.65 € Tax Included

88.65 € Tax Included

(0.00 € / Units)
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Instrument

What is the Black Line Posterior Periotome #1?

The Black Line Posterior Periotome #1 is a precision instrument designed by the manufacturer Hu-Friedy for oral surgery. This device is distinguished by its specific configuration adapted to the posterior areas of the oral cavity. Part of the Black Line range, this instrument features a dark finish that reduces reflections under operatory lighting, thus optimizing the practitioner's visual comfort. Its structure is designed to be delicately inserted into the ligament space to prepare for tooth extraction. As a product developed by Hu-Friedy Mfg. Co., LLC, it meets the manufacturing standards of a recognized leader in the dental sector.

What are the clinical indications for this instrument?

The Posterior Periotome #1 is primarily indicated during tooth extraction procedures, particularly in the context of implant surgeries where the preservation of the alveolar bone is critical. Its role is to section the fibers of the periodontal ligament in a targeted manner. By using this instrument in posterior sectors, the dental surgeon can mobilize the tooth with reduced stress on the surrounding bone walls. This use is fundamental for maintaining the integrity of the bone plate, thereby facilitating immediate or delayed implant placement. Hu-Friedy instrumentation here serves a rigorous surgical approach.

What are the technical characteristics of the Black Line Periotome #1?

This Class I medical device features technical characteristics optimized for access to molars and premolars. The specificity of the Posterior #1 model lies in the angulation of its working part, allowing difficult-to-access areas to be reached with constant precision. The Black Line range from Hu-Friedy incorporates a high-performance coating that improves the contrast between the instrument and the soft or hard tissues. This technical design aims to offer fine handling during ligament syndesmotomy. The quality of the assembly guarantees a direct transmission of the force applied by the practitioner during insertion into the sulcus.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, general contraindications related to the use of manual instruments in oral surgery apply. Although the raw MDR text mentions the existence of indications and contraindications, no specific pathology or allergy is exhaustively listed in the source data. It is the responsibility of the healthcare professional to evaluate the patient's clinical status before any intervention. Use should be avoided if anatomical conditions do not allow for a safe passage of the periotome blade or if the practitioner judges that the instrument is not adapted to the root morphology concerned.

What are the precautions for use for this non-resorbable instrument?

As a reusable and non-resorbable surgical instrument, the Posterior Periotome #1 requires a strict sterilization protocol between each patient. It is imperative to follow the cleaning and disinfection instructions recommended by Hu-Friedy to maintain the integrity of the Black Line coating and the sharpness of the blade. The practitioner must inspect the instrument before each use to detect any signs of wear or deformation. Inappropriate handling, such as the application of excessive lateral force, could damage the fine working part. Careful reading of the instructions for use before the first commissioning is a mandatory step to ensure operational safety.

Who is the manufacturer and what standards are respected?

The Black Line Posterior Periotome #1 is manufactured by Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This medical device is listed under Class I, in accordance with the current regulations on medical devices. As a Class I product, it meets the safety and performance requirements defined for this category of manual surgical instruments. The manufacturer specifies that the use of this tool is strictly reserved for qualified healthcare professionals. Compliance with manufacturing standards by Hu-Friedy ensures clinicians a reliable instrument for their daily interventions in periodontal and implant surgery.


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Specifications

Manufacturer Hu-Friedy
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