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Lucas #88 Black Line surgical curette 4.7mm - Hu-Friedy - Delynov

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The Curette chirurgicale Lucas #88 Black Line 4,7mm - Hu-Friedy 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.

127.35 € 127.35 EUR 127.35 € Tax Included

127.35 € Tax Included

(0.00 € / Units)
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Instrument

What is the Lucas #88 Black Line 4.7mm surgical curette?

The Lucas #88 Black Line surgical curette is a precision instrument manufactured by Hu-Friedy, specifically designed for oral and implant surgery procedures. This model is distinguished by its 4.7mm working end and its membership in the Hu-Friedy Black Line range, which features a dark coating optimizing visual contrast in the mouth. As an alveolar curette, it features a robust structure suitable for curettage of hard and soft tissues, thus facilitating the rigorous cleaning of operative sites. Its design is studied to meet the requirements of practitioners looking for a reliable instrument for the management of sockets and bone defects.

What are the clinical indications for this instrument?

This Lucas curette is primarily indicated for post-extraction alveolar curettage. It allows the dental surgeon or implantologist to effectively remove inflammatory tissue, dental debris, or granulation tissue present in the socket. It is also used for the enucleation of periapical cysts or the debridement of deep periodontal lesions. Its 4.7mm size makes it particularly suitable for areas requiring wide access for complete cleaning of the bone cavity. The use of this Hu-Friedy instrument is strictly reserved for healthcare professionals trained in oral surgery techniques.

What are the technical characteristics of the Lucas #88 curette?

The Lucas #88 Black Line surgical curette has a 4.7mm working end, an ideal dimension for treating molar sockets or large debridement areas. It is part of the technical range developed by Hu-Friedy Mfg. Co., LLC, integrating Black Line technology. This technical specificity aims to improve visibility during the surgical procedure by reducing light reflections. Although material details are not specified, the design meets the brand's quality standards to ensure effective force transmission during the curettage of calcified or fibrous tissues.

What are the contraindications for the use of this curette?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific listed medical contraindications other than the use reserved exclusively for qualified healthcare professionals. As with any surgical instrument, use is contraindicated if the practitioner judges that the morphology of the operative site or the general health of the patient does not allow for a safe surgical intervention. It is necessary to systematically refer to the instructions for use and respect sterilization protocols before any clinical application to avoid any risk of cross-contamination.

What are the precautions for use and maintenance?

The Lucas #88 Black Line alveolar curette is a Class I medical device that requires rigorous handling. Before each use, it is imperative to carefully read the instructions provided by Hu-Friedy. The practitioner must ensure the integrity of the instrument and its perfect sterility. Although this device is not absorbable like a suture, its longevity depends on compliance with the cleaning and sterilization cycles recommended by the manufacturer. Particular attention must be paid to the Black Line coating to preserve its visual properties throughout its use in the dental office or operating room.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device according to current regulations. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its surgical instrumentation. Compliance with Class I ensures that the device meets the safety and performance requirements for non-invasive or invasive instruments for temporary use. The practitioner must ensure that this instrument is used in accordance with the intended use defined by the manufacturer to guarantee patient safety.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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