Gracey Curette No. 17/18 Handle No. 2 Distal - Hu-Friedy
The Excavateur #18H manche #6 renforcé - 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.
What is the Hu-Friedy #18H excavator?
The #18H excavator from the brand Hu-Friedy is a specific manual instrument used in dentistry and oral surgery. This model is distinguished by its reinforced #6 handle, offering a robust structure for practitioners. Manufactured by Hu-Friedy Mfg. Co., LLC, this device is designed to meet the requirements of daily clinical interventions. As an instrument in the INSTRU category, it features a configuration suitable for manual tissue removal. Its structure allows for efficient transmission of force during curettage or excavation of altered dental tissues, ensuring controlled handling by the dental surgeon.
What are the clinical indications for this instrument?
The #18H excavator is primarily indicated for the removal of softened dentin during the treatment of carious lesions. In oral and endodontic surgery, it can be used for the removal of debris, granulation tissue, or for cleaning access cavities. Its specific shape allows it to reach cavity walls and retention areas with precision. This Hu-Friedy instrument is an essential tool for cavity preparation before placing restorative materials. It is also suitable for certain stages of periodontal or peri-apical curettage according to the specific needs of the surgical intervention carried out by the healthcare professional.
What are the technical characteristics of the reinforced #6 handle?
The reinforced #6 handle equipped on this Hu-Friedy excavator is designed to offer ergonomics adapted to the needs of surgeons. Its reinforced design ensures increased durability when applying the mechanical pressures necessary for the excavation of calcified or softened tissues. This type of handle allows for a stable grip, limiting fatigue during prolonged procedures. The surface finish is designed to maintain rigorous hygiene in the office. This device belongs to Class I of medical devices, which confirms its compliance with the basic regulatory requirements for non-invasive or invasive instruments for temporary use used in dental practice.
What are the contraindications for the use of this excavator?
The use of the Hu-Friedy #18H excavator must be limited to the clinical indications provided by the manufacturer. Although the source text does not list specific medical contraindications related to systemic pathologies, the instrument must not be used for tasks other than those for which it was designed, such as lifting heavy bone structures or applying excessive torsional forces that could damage the working end. It is imperative that the user be a qualified healthcare professional. Any use on healthy tissues not intended to be excavated is contraindicated to preserve the structural integrity of the tooth or surrounding tissues.
What are the maintenance and sterilization precautions?
As a Class I instrument manufactured by Hu-Friedy, the #18H excavator must be subjected to a strict cleaning and sterilization protocol before each use. It is reserved for healthcare professionals who must read the instructions carefully before any handling. Precautions include visual inspection of the instrument to detect any sign of wear or corrosion on the #6 handle or the active end. Improper maintenance can compromise the performance of the instrument and patient safety. Compliance with the sterilization cycles recommended by the manufacturer Hu-Friedy Mfg. Co., LLC is essential to guarantee the longevity of the steel and asepsis during surgical interventions.
Who is the manufacturer and what standards are respected?
The #18H excavator is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is recognized worldwide for the quality of its dental instrumentation. This product is classified as a Class I medical device according to current regulations. Although specific CE marking is not mentioned in the source data, compliance with Hu-Friedy manufacturing standards ensures rigorous traceability and production quality. Healthcare professionals must refer to the instructions provided by the manufacturer to ensure use in accordance with the safety and clinical efficacy standards expected for this type of surgical instrument.
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Specifications
| Manufacturer | Hu-Friedy |
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