Instrument for composite fillings, Hu-Friedy n°2 handle n°41 molars - Hu-Friedy - Delynov
The Instrument à composite Hu-Friedy #2 manche #41 Molaires - 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 composite instrument #2 handle #41 Molars?
The Hu-Friedy composite instrument #2 with #41 handle is a manual device designed by Hu-Friedy Mfg. Co., LLC for restorative dentistry procedures. This medical device belongs to the instrument category (INSTRU) and is distinguished by a structure adapted for work on molars. It allows practitioners to manipulate composite materials with precision. As a Class I product, it meets the basic regulatory requirements for reusable non-invasive instruments. Its design integrates a specific handle, referenced under number #41, offering a grip adapted to prolonged clinical interventions in the posterior zone.
What are the clinical indications?
This instrument is indicated for the shaping and modeling of composite resins during Class I, II, and other cavity restorations involving molars. In restorative dental surgery, it is used to condense the material, sculpt the occlusal anatomy, and adjust marginal ridges. Its use is particularly relevant for ensuring precise adaptation of the composite to the cavity walls, thereby limiting the risk of bubbles or sealing defects. The manufacturer Hu-Friedy specifies that this device is exclusively reserved for qualified healthcare professionals, guaranteeing use in accordance with current clinical protocols in dental offices and care centers.
What are the technical characteristics?
The Hu-Friedy composite instrument #2 is characterized by a double or single working end, specifically sized for molars. The #41 handle is a central technical component of this model, offering ergonomics designed for control of movement when applying moderate pressure on restorative materials. Manufactured by Hu-Friedy Mfg. Co., LLC, this device is classified as Class I according to medical device regulations. Hu-Friedy's manufacturing quality ensures resistance to standard sterilization cycles in medical environments. Although exact material details are not specified in the raw technical data, the design aims for neutrality toward resins to prevent composite adhesion.
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, other than those related to use by unqualified personnel. The regulatory text emphasizes that use is strictly reserved for healthcare professionals. It is imperative to read the instructions for use carefully before any intervention to become aware of the manufacturer's warnings. As with any Class I instrument, a visual inspection before use is recommended to ensure the integrity of the instrument. Any use diverted from its primary function of composite modeling could alter its technical performance.
What are the maintenance and durability precautions?
As a Class I instrument intended for professional use, the Hu-Friedy composite instrument #2 must be subjected to standard cleaning, disinfection, and sterilization protocols between each patient. Although resorption specifications do not apply here as it is a manual non-implantable instrument, its durability depends on compliance with Hu-Friedy maintenance instructions. Appropriate cleaning solutions should be used to avoid any corrosion or degradation of the #41 handle. Storage must be in a dry and clean environment. Compliance with these steps guarantees the maintenance of the instrument's functional properties during restorative procedures on molars.
Who is the manufacturer and what standards are met?
The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This company is a recognized manufacturer in the dental sector for the quality of its surgical and restorative instruments. The product is listed under Class I of medical devices. Compliance with standards is ensured by the manufacturer, although the specific CE marking is not mentioned in the provided source data. Professionals must refer to the attached instructions for use to validate implementation protocols. Hu-Friedy imposes a strict framework for use, reminding that this equipment is exclusively intended for use by trained healthcare practitioners.
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Specifications
| Manufacturer | Hu-Friedy |
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