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McCall curette #17/18 handle #6

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The Curette McCall #17/18 manche #6 is a medical device manufactured by le fabricant.

  • Compliance: Medical device Class I.
  • Manufacturer: le fabricant.
  • Reserved for healthcare professionals. Read instructions carefully before use.

69.15 € 69.15 EUR 69.15 € Tax Included

69.15 € Tax Included

(0.00 € / Units)
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Instrument

What is the McCall #17/18 curette handle #6?

The McCall #17/18 curette handle #6, distributed by the brand Hu-Friedy, is a manual instrument specific to periodontology. This medical device consists of a double working end mounted on a #6 type handle. Its structure is designed to offer a grip adapted to the requirements of dental surgeons during deep hygiene care. Manufactured under the supervision of the manufacturer, this instrument belongs to the INSTRU category. It meets the needs for cleaning dental and root surfaces within a strict clinical framework. The brand Hu-Friedy ensures that this tool meets professional standards for interventions in dental offices or hospital environments.

What are the clinical indications?

The clinical indications for this instrument from the brand Hu-Friedy primarily concern non-surgical and surgical periodontal therapy. The McCall #17/18 curette is indicated for deep scaling and root planing. It is used to remove calcified calculus and necrotic tissue from the surface of dental roots inside periodontal pockets. This action is crucial for promoting epithelial reattachment and reducing gingival inflammation. The intended use, as defined by the manufacturer Hu-friedy, limits the use of this device to qualified healthcare professionals mastering periodontal curettage techniques.

What are the technical characteristics?

The McCall #17/18 curette is distinguished by its #6 handle configuration, offering a specific volume for the practitioner's comfort during repetitive procedures. The design of the #17/18 active part is specifically angled to allow optimal access to the distal and mesial surfaces of posterior teeth. As a Class I device, it complies with basic regulatory requirements for non-invasive or invasive instruments for temporary use. The manufacturer Hu-friedy, based in Chicago, ensures production compliance. Although material details are not specified, the instrument is designed to withstand standard sterilization cycles in effect in dental asepsis protocols.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not exhaustively listed beyond the standard usage warnings. However, the use of this instrument is strictly reserved for healthcare professionals. An implicit contraindication lies in use by untrained personnel, which could result in damage to soft tissues or the cementum structure of the tooth. It is imperative to consult the instructions before use to identify any restrictions related to the patient's clinical status or particular precautions for use. Compliance with sterilization protocols is also a sine qua non condition to avoid any risk of cross-infection.

What are the maintenance and durability precautions?

As a non-resorbable Class I instrument, the durability of the McCall #17/18 curette depends directly on the maintenance protocols applied by the practice. Although the exact composition is not specified, this type of instrumentation from the brand Hu-Friedy requires rigorous cleaning after each intervention to remove organic debris. The sterilization process must follow the recommendations of the manufacturer Hu-friedy to preserve the integrity of the sharp edges of the #17/18 ends. Regular sharpening by a professional or with appropriate equipment may be necessary to maintain cutting efficiency during root planing, while ensuring that the initial geometry of the instrument is not altered.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device, which implies that it meets the safety and performance requirements defined for this regulatory category. Distribution is handled under the brand Hu-Friedy. In accordance with the MDR regulation and manufacturer warnings, this instrument is exclusively reserved for healthcare professionals. It is essential to carefully read the instructions provided before any commissioning. Although CE marking is not explicitly specified in the source data, traceability is ensured by the references of the American manufacturer Hu-friedy.


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Specifications

Manufacturer Hu-Friedy
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