Cassette DIN for CompoSculp Instruments - Hu-Friedy - Delynov
The Cléoïde-discoïde #90B manche #41 - 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 Cleoid-Discoid #90B handle #41 - Hu-Friedy?
The Cleoid-Discoid #90B with handle #41 is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This cleoid-discoid instrument features a double active end mounted on an ergonomic handle type #41. It belongs to the category of restorative instruments (INSTRU) and is classified as a Class I medical device. Its bipolar structure allows the practitioner to have two complementary working shapes on a single handle, thus optimizing efficiency during the shaping stages of filling materials. Hu-Friedy manufacturing quality ensures resistance adapted to the constraints of daily clinical practice in a dental office.
What are the clinical indications for this dental cleoid-discoid instrument?
This dental cleoid-discoid instrument is specifically indicated for the carving and shaping of restorative materials, such as amalgams or composites, before their complete hardening. In conservative surgery, it is used to recreate the functional anatomy of posterior teeth. The claw-shaped end (cleoid) is ideal for carving grooves and occlusal pits with precision. The circular end (discoid) allows for smoothing surfaces and removing excess material at the cavity margins. Its use is strictly reserved for healthcare professionals trained in dental restoration techniques, in accordance with the guidelines provided by the manufacturer Hu-Friedy.
What are the technical characteristics of the #41 handle?
The #41 handle equipped on this Hu-Friedy model is designed to provide a stable grip and optimal tactile control during delicate phases of occlusal carving. Although specific materials are not detailed in the source data, the design of this handle meets the requirements for Class I devices for repeated use in a clinical environment. The double-ended configuration allows for a quick transition between the cleoid tip and the discoid face without changing instruments, which reduces operative time. The technical reference #90B defines the curvature and size of the active parts, ensuring a perfect fit with the anatomical shaping needs of small and medium-sized restorations.
What are the contraindications for the use of this instrument?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than the mandatory compliance with current sterilization and asepsis protocols. The instrument must not be used for applications other than those intended by the manufacturer, notably prying on bone structures or fixed prosthetics, which could damage the active ends. Practitioners must refer to the instructions for use before any manipulation to ensure patient safety and device longevity.
What are the maintenance precautions for this Class I device?
As a Class I device manufactured by Hu-Friedy, this instrument must undergo a rigorous cleaning and sterilization cycle between each patient. Although composition details are not specified, standard maintenance for instruments in this category involves the use of pH-neutral cleaning solutions to avoid any surface alteration. It is crucial to regularly inspect the cleoid and discoid ends to detect any sign of wear or deformation that could compromise carving precision. Compliance with the manufacturer's warnings located at 3232 N. Rockwell St. Chicago, USA, is essential to maintain the technical integrity of the instrument over the long term.
Who is the manufacturer and what standards are respected by this product?
The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, a recognized company located in Chicago, USA. This medical device is listed under Class I, which corresponds to the safety and performance standards for non-invasive manual instruments in dentistry. Although specific CE marking is not mentioned in the source data, the product meets the regulatory requirements of its class for professional marketing. The warnings and instructions for use provided by Hu-Friedy emphasize that use is exclusively reserved for healthcare professionals. Each practitioner must carefully read the manual to ensure their use complies with current clinical standards.
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Specifications
| Manufacturer | Hu-Friedy |
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