Sugarman File #1S/2S #2 Handle - Hu-Friedy - Delynov
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.
| Manufacturer: Hu-Friedy |
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What is the Sugarman #1S/2S file handle #2 - Hu-Friedy?
La lime Sugarman #1S/2S est un instrument de précision fabriqué par Hu-Friedy Mfg. Co., LLC. Ce dispositif se compose d'une partie travaillante spécifique et d'un manche de type #2, optimisé pour la manipulation lors des interventions chirurgicales. En tant qu'instrument de la catégorie INSTRU, il répond aux exigences de qualité d'un fabricant reconnu dans le domaine de l'instrumentation chirurgicale orale et parodontale. Ce modèle est spécifiquement conçu pour apporter une réponse adaptée aux besoins des chirurgiens oraux et des implantologues durant les phases de rectification osseuse. Sa structure permet un accès aux zones interproximales avec une efficacité constante.
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?
Techniquement, la curette Sugarman #1S/2S se distingue par sa configuration de manche #2, offrant une prise stable pour les mouvements de raclage et de lissage. Sa fabrication par Hu-Friedy garantit la conformité aux standards industriels pour les instruments de Classe I. Sa conception à double extrémité permet de traiter différentes angulations lors des interventions sur le bloc alvéolaire. L'instrument est conçu pour résister aux cycles de stérilisation standard en chirurgie orale, assurant ainsi une longévité conforme aux attentes des plateformes techniques chirurgicales.
What are the contraindications for the use of this device?
Aucune contre-indication spécifique n'est listée de manière exhaustive au-delà des avertissements d'utilisation. L'utilisation de cet instrument est strictement réservée aux professionnels de santé formés. La lime de Sugarman ne doit pas être utilisée en dehors de son usage prévu, à savoir la chirurgie orale et parodontale. Les praticiens doivent évaluer les risques individuels pour chaque patient, particulièrement en cas de fragilité osseuse excessive ou de pathologies systémiques pouvant compromettre la cicatrisation post-opératoire. Une lecture attentive des instructions avant utilisation est impérative.
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.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
