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Sugarman File #1S/2S #2 Handle - Hu-Friedy - Delynov

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The Lime Sugarman #1S/2S manche #2 - 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.

114.75 € 114.75 EUR 114.75 € Tax Included

114.75 € Tax Included

(0.00 € / Units)
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Instrument

What is the Sugarman #1S/2S file handle #2 - Hu-Friedy?

The Sugarman #1S/2S file is a precision instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device consists of a specific working part and a #2 type handle, optimized for handling during surgical interventions. As an instrument in the INSTRU category, it meets the quality requirements of a recognized manufacturer in the field of dental and periodontal instrumentation. This model is specifically designed to provide a response adapted to the needs of dental surgeons and implantologists during bone rectification phases. Its structure allows access to interproximal areas with consistent efficiency.

What are the clinical indications for this instrument?

The intended use of the Sugarman file is primarily oriented towards periodontal surgery and oral surgery. It is indicated for smoothing bone surfaces after an osteotomy or osteoplasty, as well as for the removal of inflammatory tissue in infra-bony defects. Practitioners use this instrument to refine alveolar contours and prepare the site before implant placement or guided tissue regeneration. In accordance with Hu-Friedy guidelines, this device is exclusively reserved for qualified healthcare professionals, ensuring use compliant with current clinical protocols in implantology and periodontology.

What are the technical characteristics of the Sugarman file?

Technically, the Sugarman #1S/2S file is distinguished by its #2 handle configuration, offering a stable grip for scraping and smoothing movements. Although the exact composition is not specified in the source data, manufacturing by Hu-Friedy guarantees compliance with industrial standards for Class I instruments. Its double-ended design allows for treating different angulations during interventions on the alveolar block. The instrument is designed to withstand standard sterilization cycles in the dental office, thus ensuring longevity consistent with the expectations of surgical technical platforms.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not listed exhaustively beyond the warnings for use. However, the use of this instrument is strictly reserved for trained healthcare professionals. The Sugarman file should not be used outside of its intended use, namely oral and periodontal surgery. Practitioners must assess individual risks for each patient, particularly in cases of excessive bone fragility or systemic pathologies that could compromise post-operative healing. A careful reading of the instructions before use is imperative.

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

As a reusable surgical instrument and not a resorbable device like a suture, the Sugarman file requires a rigorous decontamination and sterilization protocol after each intervention. It is essential to follow Hu-Friedy instructions regarding cleaning to avoid any corrosion or accumulation of organic debris in the file's serrations. Maintaining the integrity of the working part is crucial to guarantee the efficiency of bone smoothing. Professionals must inspect the instrument before each use to detect any signs of wear or deformation that could alter the precision of the surgical gesture.

Who is the manufacturer and what standards are respected?

The Sugarman #1S/2S file is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer Hu-Friedy is a historical and recognized player for the quality of its surgical instruments. Although specific CE marking is not mentioned in the current technical sheet, the product complies with regulatory requirements for devices of its class. It is reminded that this equipment is intended exclusively for professional use and that it is essential to consult the attached technical instructions before any clinical handling.


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Specifications

Manufacturer Hu-Friedy
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