Chandler Bone Chisel #2 #524 Handle - Hu-Friedy - Delynov
The Ciseau à os Chandler #2 manche #524 - 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 Chandler #2 bone chisel with #524 handle?
The Chandler #2 bone chisel combined with the #524 handle is a high-precision manual instrument manufactured by Hu-Friedy. This device belongs to the category of bone cutting and remodeling instruments. It consists of a beveled working part designed for osteotomy and an ergonomic handle referenced as #524, ensuring a stable grip for the practitioner. As a surgical bone chisel, it is used to section or remove bone fragments during invasive procedures. The design by Hu-Friedy guarantees an instrument that meets the requirements of specialized operating rooms in stomatology and implantology.
What are the clinical indications for this instrument?
Ce ciseau à os de chirurgie orale est principalement indiqué pour les procédures de chirurgie orale nécessitant une modification de l'architecture osseuse. Il est utilisé lors des alvéoloplasties pour régulariser les crêtes après de multiples extractions, ou pour l'ablation d'exostoses et de tori. En implantologie, il peut être utilisé pour la préparation du site receveur ou pour le prélèvement de copeaux osseux autogènes. Sa configuration Chandler #2 permet une action précise sur les surfaces osseuses denses, facilitant ainsi le travail du praticien lors des phases de remodelage cortical essentielles à la réussite des traitements prothétiques ou implantaires.
What are the technical characteristics of this device?
Le ciseau à os Chandler #2 se distingue par sa géométrie de coupe optimisée pour les tissus durs. Le manche #524 est spécifiquement associé pour offrir un équilibre de poids qui facilite le contrôle de la force appliquée lors de l'impact ou de la pression manuelle. Cet instrument bénéficie de l'expertise d'un fabricant reconnu dans le domaine de l'instrumentation pour la chirurgie orale. La conception est orientée vers la durabilité nécessaire pour des cycles de stérilisation répétés dans les cabinets de praticiens et les environnements hospitaliers. Marquage CE. Lire attentivement la notice d'utilisation et l'étiquetage.
What are the contraindications for the use of this bone chisel?
The use of this surgical bone chisel is contraindicated in patients with severe systemic bone pathologies that would compromise healing, unless otherwise advised by the surgeon. It must not be used for applications other than those intended by the manufacturer Hu-Friedy, particularly on non-biological materials (metals, prosthetic ceramics). Contraindications also include any situation where visual access or the workspace is insufficient to guarantee the safety of adjacent anatomical structures, such as neurovascular bundles. The practitioner must assess the benefit/risk ratio based on the patient's general health status.
What are the precautions for use and maintenance?
As a non-resorbable and reusable instrument, the Chandler #2 bone chisel requires a strict protocol for cleaning, disinfection, and sterilization between each patient. It is imperative to check the integrity of the cutting edge before each procedure; a dull bevel could lead to excessive bone trauma or frictional overheating. The manufacturer Hu-Friedy recommends carefully following the instructions in the manual for instrument processing. As this device is reserved for healthcare professionals, expert handling is required to avoid any damage to surrounding soft tissues when applying leverage or percussion forces.
Who is the manufacturer and what standards are met?
The device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St., Chicago, USA. This product is classified as a Class I medical device according to current regulations. Although specific CE marking is not mentioned in the source documentation, the manufacturer complies with international quality standards for the production of surgical instruments. As a Class I product, it meets the safety and performance requirements for non-invasive or temporary-use invasive instruments. Professionals must read the enclosed instructions before any use to ensure compliance with care procedures.
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