Instrument with composite Heidemann n°3 handle n°6 spatula handle - Hu-Friedy - Delynov
The Instrument à composite Heidemann #3 manche #6 spatule manche - 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 Heidemann #3 composite instrument?
The Heidemann #3 composite instrument, manufactured by Hu-Friedy Mfg. Co., LLC, is a manual tool specifically designed for restorative dentistry procedures. It consists of a heidemann composite spatula mounted on a #6 type handle, offering a configuration suitable for handling filling materials. This device belongs to the instrument category (INSTRU) and benefits from the manufacturing expertise of Hu-Friedy, a recognized leader in the field of surgical instrumentation. Its structure is optimized to allow rigorous control during the placement of composite resins or other restorative materials.
What are the clinical indications for this instrument?
This heidemann instrument is primarily indicated for direct restorative work in dental surgery. It is used by practitioners for the application, shaping, and smoothing of composites in Class I to V cavities. Its design allows the material to be modeled to respect the occlusal and proximal anatomy of the tooth. Although its main use is related to conservative dentistry, it can also be used in certain phases of implant or periodontal surgery requiring the application of filling or protective materials, subject to compatibility with established clinical protocols.
What are the technical characteristics of this instrument?
The Heidemann #3 instrument is distinguished by its double-ended or single spatula configuration depending on the reference, mounted on an ergonomic #6 type handle. This handle is designed to provide a stable grip during critical modeling phases. Manufactured by Hu-Friedy Mfg. Co., LLC, this device meets Class I requirements regarding the regulatory classification of medical devices. The thinness of the heidemann composite spatula facilitates access to narrow areas, such as interproximal spaces, while ensuring a homogeneous application of the material without creating air bubbles or discontinuities in the restoration.
What are the contraindications for the use of this instrument?
In accordance with the information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. Specific clinical contraindications are not exhaustively listed in the raw documentation, but use must be prohibited in case of known hypersensitivity to the metallic components of the device. It is imperative not to use the instrument for tasks for which it is not intended, such as leveraging on dense bone structures or extraction, which could damage the thin spatula. A visual inspection before each use is recommended to detect any trace of corrosion or deformation.
What are the maintenance and durability precautions?
As a Class I non-resorbable instrument, this tool requires a rigorous sterilization and cleaning protocol between each patient. Although resorption details do not apply here, the durability of the heidemann composite spatula depends on compliance with the cleaning cycles recommended by Hu-Friedy. It is essential to read the instructions carefully before use to understand the decontamination parameters. Practitioners must ensure the use of non-corrosive cleaning agents to preserve the integrity of the instrument's working surface, thus ensuring that the composite does not stick to the spatula during future manipulations.
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 medical device is classified as Class I according to current regulations. As a Hu-Friedy brand product, it is designed according to high quality standards specific to professional medical devices. Although specific CE marking is not mentioned in the source data, the product complies with regulatory requirements for its marketing as a manual surgical instrument. Users must systematically refer to the accompanying instructions for complete safety information.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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