Loma Linda #10/11 curette #6 handle
The Curette Loma Linda #10/11 manche #6 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.
What is the Loma Linda #10/11 curette handle #6?
The Loma Linda #10/11 curette marketed by the Hu-Friedy is a specific manual instrument intended for periodontology and oral surgery. This device is distinguished by its double active end numbered 10/11, mounted on a type #6 handle. This handle features an optimized diameter to offer a rigorous grip for practitioners during curettage phases. Manufactured under the supervision of the manufacturer Hu-Friedy, this instrument from the INSTRU category meets the quality requirements necessary for clinical interventions in dental offices or hospital environments. Its architecture is designed to allow precise access to difficult periodontal areas, thus facilitating the work of the dental surgeon during initial or surgical treatment phases.
What are the clinical indications?
The loma linda curette is mainly indicated for the treatment of periodontal diseases. It is used for deep scaling and root planing, allowing the removal of calcified deposits and bacterial biofilm located in periodontal pockets. In implant or oral surgery, it is also used for the debridement of inflammatory tissues and the preparation of bone or root surfaces before guided tissue regeneration. This Hu-Friedy device is an essential tool for sanitizing surgical sites, thus ensuring an environment conducive to healing. Its use is strictly reserved for qualified health professionals mastering manual curettage techniques.
What are the technical characteristics?
Technically, this Hu-Friedy instrument consists of a rigid shank and two specific working ends with the Loma Linda #10/11 design. The handle #6 is designed to reduce muscle fatigue during prolonged use thanks to its ergonomics adapted to the practitioner's hand. As a Class I device, it complies with regulatory standards for non-invasive or short-term invasive instruments. The design by the manufacturer Hu-Friedy ensures a precise finish of the active parts, allowing an effective cutting edge for the removal of pathological tissues. The lack of material specification in the source data limits the description to the functional and structural aspects of the handle and tips.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is exclusively reserved for health professionals. There are no specific medical contraindications listed in the raw technical documentation, except for those related to inappropriate practice or use by untrained personnel. As with any sharp manual instrument, its use should be avoided if the integrity of the instrument is compromised or if the patient's morphology does not allow safe access without the risk of damaging critical anatomical structures. It is imperative to read the instructions carefully before any use to guarantee the safety of the patient and the practitioner.
What are the maintenance and durability precautions?
As a non-resorbable Class I instrument, the Loma Linda curette requires a rigorous sterilization and cleaning protocol between each patient. Although material details are not specified, maintenance of Hu-Friedy instruments generally involves decontamination, ultrasonic or manual cleaning, followed by autoclave sterilization. The sharpness of the #10/11 ends should be checked regularly to maintain curettage efficiency. Inadequate maintenance can alter the cutting performance and longevity of the device. Professionals must refer to the reprocessing instructions provided by the manufacturer to ensure compliance with current hygiene standards.
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 according to the regulations in force. Although the CE marking is not explicitly specified in the source data, manufacturing by a recognized player in the dental sector guarantees compliance with industrial health standards. The instrument is intended for strict professional use in dental and periodontal surgery. Any use must be preceded by a careful reading of the instructions for use to respect the safety recommendations and clinical protocols established by the manufacturer.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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