Cushing scaler #61 handle #1 bone chisel
The Détartreur Cushing #61 manche #1 ciseau à os is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Hu-Friedy |
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What is the Cushing #61 scaler handle #1 bone chisel?
The Cushing #61 scaler, offered by the brand Hu-Friedy, is a manual instrument designed for bone surgery interventions. This device is distinguished by its specific configuration combining the properties of a scaler and a manual bone chisel. Its structure is based on a #1 type handle, offering a grip adapted to precision movements during the manipulation of hard tissues. Manufactured under the supervision of the manufacturer Hu-friedy, this instrument belongs to the INSTRU category and meets the requirements of Class I. It is specifically developed to meet the needs of practitioners performing complex bone instrumentation acts in a clinical setting.
What are the clinical indications?
This instrument from the brand Hu-Friedy is indicated for oral surgery procedures requiring action on bone tissues. Its primary use concerns bone instrumentation, including resection, scraping, or remodeling of cortical surfaces. In implant or periodontal surgery, the bone chisel allows for the preparation of the surgical site by removing bone irregularities or harvesting autogenous bone chips. The intended use by the manufacturer Hu-friedy strictly limits the use of this device to qualified healthcare professionals, thus guaranteeing an application compliant with current clinical standards.
What are the technical characteristics?
The Cushing #61 scaler is characterized by its specific technical reference within the Hu-Friedy brand catalog. Equipped with a #1 handle, it offers ergonomics adapted to the pressures exerted during the bone cutting or curettage phases. As a manual bone chisel, it requires no external power source, allowing the surgeon direct tactile feedback during interaction with the bone. Although material details are not specified, manufacturing by Hu-friedy in the USA ensures compliance with production protocols for Class I devices. Its design is optimized for durability and resistance to repeated sterilization cycles.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, there are no specific medical contraindications listed for this instrument, beyond standard oral surgery protocols. However, the use of this bone chisel is strictly reserved for trained healthcare professionals. Improper handling or use on unsuitable anatomical structures could lead to tissue damage. It is imperative to read the instructions carefully before any use to ensure the suitability between the instrument and the planned surgical act, while respecting the rigorous aseptic conditions specific to the operating room.
What are the maintenance and usage precautions?
Being a non-resorbable instrument intended for repeated use, this device from the brand Hu-Friedy requires a strict decontamination and sterilization protocol after each intervention. Usage precautions include a visual inspection of the working end of the manual bone chisel to detect any wear or dullness that could compromise cutting efficiency. Storage must be carried out in a dry and clean environment to preserve the integrity of the bone instrumentation. Compliance with the cleaning instructions provided by the manufacturer Hu-friedy is essential to maintain the performance of the Class I instrument over the long term.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device, which implies compliance with safety and performance regulations for non-invasive or reusable surgical instruments. The brand Hu-Friedy ensures the distribution of this high-quality bone instrumentation tool. Although the CE marking is not specified in the source documentation, the device follows rigorous American manufacturing standards. It is reminded that this instrument is exclusively reserved for healthcare professionals and that the instructions must be consulted before use.
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