Elevator Roy Handle Number 510 Reversed - Hu-Friedy - Delynov
The Elévateur Roy manche #510 inversé - 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 Roy elevator #510 inverted handle - Hu-Friedy?
L'élévateur Roy #510 à manche inversé est un instrument manuel spécialisé. Ce dispositif chirurgical se distingue par sa configuration de manche spécifique numéro 510, orientée de manière inversée pour répondre à des besoins ergonomiques et cliniques précis en chirurgie orale. En tant qu'instrument de la catégorie INSTRU, il est destiné à la manipulation des structures radiculaires et des tissus durs. Ce produit est fabriqué par Hu-Friedy, un acteur reconnu dans le domaine de l'instrumentation médicale, garantissant une conception adaptée aux exigences des blocs opératoires et des cabinets de chirurgie orale.
What are the clinical indications for this instrument?
This inverted dental elevator is primarily indicated for exodontia procedures. Its clinical use focuses on the luxation of teeth and the elevation of roots prior to forceps extraction. It is particularly useful in situations where the root anatomy or the position of the tooth requires a specific leverage that only a Roy elevator with an inverted orientation can provide. The instrument allows for the breaking of periodontal ligament fibers and the widening of the socket, thus facilitating the removal of the tooth or root debris during alveolar surgeries or pre-implant preparations.
What are the technical characteristics of this elevator?
The Hu-Friedy Roy elevator features technical characteristics defined by its #510 handle in an inverted version. Although the exact material composition is not specified in the source data, the instrument meets the manufacturing standards of Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. It is a robust device designed to withstand the torsional and leverage forces required for root elevation. Its regulatory classification as a Class I device confirms its status as a non-invasive or short-term invasive surgical instrument, suitable for repeated use after appropriate sterilization according to current protocols.
What are the contraindications for the use of this Roy elevator?
Aucune contre-indication spécifique n'est détaillée au-delà des avertissements généraux. L'utilisation de cet instrument est strictement réservée aux professionnels de santé qualifiés. L'instrument ne doit pas être utilisé pour des tâches autres que son usage prévu (élévation et luxation en chirurgie orale). Les praticiens doivent évaluer les risques en fonction de l'état de santé général du patient et de la fragilité des structures osseuses environnantes. Comme indiqué dans la notice d'utilisation, une lecture attentive des instructions avant usage est impérative pour garantir la sécurité du patient et la longévité de l'outil.
What are the precautions for use and maintenance?
The use of this Roy inverted elevator requires thorough knowledge of oral surgery techniques to avoid any unwanted bone or root fractures. As a reusable instrument, it must be cleaned, disinfected, and sterilized between each patient in accordance with Hu-Friedy guidelines. It is essential to check the integrity of the working part and the handle before each intervention. Compliance with sterilization protocols is crucial to maintain the mechanical properties of the Class I instrument. Professionals must ensure the instrument is used within the limits of its structural capacities without exerting excessive force.
Who is the manufacturer and what standards are respected?
The elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, IL 60618 USA. This medical device belongs to Class I according to current regulations. The manufacturer Hu-Friedy is globally recognized for the quality of its surgical instruments. The product is intended exclusively for healthcare professionals, highlighting the requirement for technical competence for its handling. Although specific CE marking is not mentioned in the source data, compliance with US and international manufacturing standards for Class I devices is ensured by Hu-Friedy's rigorous processes.
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