Scissors for Bone Buser 6mmx135mm - Hu-Friedy - Delynov
The Couteau pour oter les excès #21 manche #6 aurification - 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 #21 excess removal knife?
The #21 excess removal knife, manufactured by Hu-Friedy, is a specialized manual instrument intended for restorative dentistry. This model is distinguished by its #6 handle with a gold-plated finish, offering a grip adapted to high-precision movements. As a restoration finishing instrument, its structure is designed to facilitate the removal of excess materials after polymerization or hardening of filling products. This device belongs to Class I of medical devices, guaranteeing its compliance with regulatory standards for non-invasive instruments used in dental offices by qualified practitioners.
What are the clinical indications for this instrument?
This composite excess knife is primarily indicated for the finishing stages of direct and indirect restorations. In dental surgery and conservative dentistry, it is used to eliminate overflows of composite, cement, or other filling materials at the enamel-restoration junctions. Its use is particularly relevant for refining anatomical contours and freeing interdental spaces from bonding residues. As a dental finishing instrument, it helps guarantee periodontal integrity by avoiding plaque retention areas caused by excess material in subgingival or interproximal zones.
What are the technical characteristics of the #6 gold-plated handle?
The Hu-Friedy #21 knife is equipped with the #6 gold-plated handle, a technical feature specific to the high-quality range from the manufacturer Hu-Friedy Mfg. Co., LLC. This handle is designed to offer an optimal balance between weight and maneuverability, reducing fatigue during prolonged composite finishing interventions. The working end of the instrument, the #21 knife, features a specific geometry allowing for clean cutting of excesses. Although the exact material composition is not specified in the source data, the Hu-Friedy design meets the durability requirements necessary for repeated cleaning and sterilization cycles in a clinical setting.
What are the contraindications for the use of this excess knife?
According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for duly trained healthcare professionals. There are no specific medical contraindications listed, other than compliance with intended use protocols. It must not be used for tasks other than the removal of restoration materials (such as bone excision or sectioning of unintended hard tissues), at the risk of damaging the working part or injuring the patient. The practitioner must systematically refer to the instructions for use and manufacturer warnings to ensure maximum safety during the operative act.
What are the maintenance and handling precautions?
Like any Class I instrument intended for dental surgery, this composite excess removal knife must be handled with care to preserve the sharpness of its #21 blade. Although this product is not a resorbable device like a suture, it requires a rigorous decontamination and sterilization protocol between each patient. Professionals must inspect the instrument before each use to detect any signs of wear or deformation. Compliance with the cleaning instructions recommended by Hu-Friedy at 3232 N. Rockwell St. Chicago is essential to maintain the performance of the restoration finishing instrument and prevent cross-contamination risks in the office.
Who is the manufacturer and what standards are met?
The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, IL 60618 USA. This excess removal knife is classified as a Class I medical device. Hu-Friedy is a globally recognized manufacturer for the quality of its dental instrumentation. The product is subject to current regulations concerning medical devices (MDR), and users are invited to read the instructions carefully before any use. The mention of Class I confirms that the instrument meets the safety and performance requirements defined for this category of professional medical devices.
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Specifications
| Manufacturer | Hu-Friedy |
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