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Curette Goldman-Fox #2 Handle #6 Special - Hu-Friedy - Delynov

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The Curette alvéolaire Molt #2/4 DE, manche #6 court - 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.

112.95 € 112.95 EUR 112.95 € Tax Included

112.95 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy Molt #2/4 DE alveolar curette?

The Molt #2/4 DE curette is a manual surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device features a double active end (DE) mounted on a short #6 handle, optimizing grip during technical maneuvers. Designed for the oral surgery environment, this curette allows for thorough cleaning of surgical sites. As an instrument in the INSTRU category, it meets the quality requirements of a recognized manufacturer in the dental sector. Its structure is specifically adapted for manipulating hard and soft tissues within the dental socket after an extraction or during the preparation of an implant site.

What are the clinical indications for this instrument?

The use of the Molt curette is primarily indicated during post-extraction phases in oral surgery. It is used for the enucleation of periapical cysts, curettage of inflammatory or infectious tissues, and removal of residual bone debris in the socket. In implantology, it is used to prepare the bone site by ensuring a clean surface, thus promoting better healing and future integration of filling materials or implants. Its double-ended design offers clinical versatility to reach difficult-to-access areas, ensuring complete debridement essential for preventing post-operative complications such as alveolar osteitis.

What are the technical characteristics of the short #6 handle?

The short #6 handle equipping this Molt curette from Hu-Friedy is specifically dimensioned to offer an optimal balance between control and maneuverability. This type of handle allows the surgeon to exert controlled pressure during the curettage of dense tissues while maintaining high tactile sensitivity. The double-ended configuration (#2/4) provides two complementary working shapes on a single instrument, thereby reducing the number of manipulations during the surgical act. Manufacturing by Hu-Friedy Mfg. Co., LLC guarantees a rigorous finish of the active parts to maintain cutting efficiency during repeated bone and periodontal surgery procedures.

What are the contraindications for the use of the Molt curette?

Contraindications for the use of the Molt #2/4 DE curette are related to the patient's general clinical conditions and standard oral surgery protocols. There are no specific absolute contraindications mentioned by the manufacturer Hu-Friedy other than use by unqualified persons. However, use should be avoided if the instrument shows signs of wear or deformation that could compromise tissue integrity or leave metallic residues. It is imperative to refer to the instructions for use provided by Hu-Friedy Mfg. Co., LLC to identify any restrictions related to the patient's health status or specific bone pathologies preventing manual instrumentation.

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

As a reusable steel surgical instrument, the Molt curette requires a strict sterilization and decontamination protocol after each use. Although the product is not a suture and is therefore not subject to resorption, its durability depends on compliance with the cleaning cycles recommended by the manufacturer. It is recommended to use non-corrosive cleaning solutions and to perform regular visual inspections of the #2/4 ends to detect any loss of efficiency. Healthcare professionals must carefully read the instructions before use to ensure that the sterilization methods applied comply with Hu-Friedy directives, thus ensuring patient safety and instrument longevity.

Who is the manufacturer and what standards are respected?

The Molt #2/4 DE alveolar curette is manufactured by Hu-Friedy Mfg. Co., LLC, a company located in Chicago, USA. This medical device belongs to Class I according to current regulations. As a Class I product, it is intended for strict professional use by dental surgeons or specialists in oral surgery. The manufacturer emphasizes that the use of this instrument is reserved exclusively for trained healthcare professionals. Compliance with Hu-Friedy manufacturing standards ensures that the instrument meets the essential safety requirements for minor invasive procedures, such as alveolar curettage and periodontal surgery.


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Specifications

Manufacturer Hu-Friedy
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