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Sculpting Instrument Tharp Number 1 with Handle Number 71 - Hu-Friedy - Delynov

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The Sculpteur Tharp #1 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.

50.85 € 50.85 EUR 50.85 € Tax Included

50.85 € Tax Included

(0.00 € / Units)
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Instrument

What is the Tharp #1 carver handle #41?

The Tharp #1 carver is a specialized manual instrument designed by the manufacturer Hu-Friedy Mfg. Co., LLC. This device consists of a specific working part and a #41 type handle, optimized for handling during clinical care. As a dental modeling instrument, it is primarily used to carve and adapt restorative materials or intervene on soft and hard tissues according to the needs of the procedure. Its design meets the quality requirements of the Hu-Friedy brand, ensuring a reliable tool for daily interventions in dental offices or hospital settings.

What are the clinical indications for the Tharp carver?

This instrument is indicated for oral surgery, periodontics, and restorative dentistry procedures. Its primary use lies in the precise modeling of filling materials or the delicate manipulation of structures during reconstruction phases. Practitioners use the Tharp #1 carver to refine anatomical contours, thus ensuring optimal functional and aesthetic integration of restorations. Although specific MDR indications are not detailed in the provided documentation, this Class I instrument is intended for healthcare professionals for technical carving and shaping maneuvers.

What are the technical characteristics of this instrument?

The Tharp #1 carver is distinguished by its #41 handle, a technical reference at Hu-Friedy offering a grip adapted to the requirements of micro-surgery and restoration. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument belongs to the INSTRU category and benefits from a Class I regulatory classification. Its structure is designed to withstand standard sterilization cycles while maintaining the integrity of its active edges. The precision of the machining allows for high tactile control, essential for modeling maneuvers that require great dexterity from the dental surgeon or implantologist.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. Contraindications are not explicitly listed in the raw MDR text, but standard clinical safety protocols should be followed. It is imperative not to use the instrument if it shows signs of degradation or obvious wear that could compromise patient safety or the effectiveness of the surgical procedure. Practitioners must consult the instructions for use before any intervention to ensure the device's suitability for the patient's clinical condition.

What are the maintenance and use precautions?

Like any Class I instrument that is non-sterile upon purchase, the Tharp #1 carver must be cleaned, disinfected, and sterilized before its first use and after each clinical use, in accordance with Hu-Friedy's instructions. It is recommended to read the manual carefully for appropriate sterilization cycles. Particular attention should be paid to inspecting the working part to maintain its modeling capabilities. Compliance with maintenance protocols guarantees the longevity of the instrument and prevents risks of cross-contamination within the dental office, while preserving the mechanical properties of the steel used by the manufacturer.

Who is the manufacturer and what standards are respected?

The Tharp #1 carver 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. Hu-Friedy is a globally recognized manufacturer in the dental sector for the rigor of its manufacturing processes and the quality of its instruments. Although specific CE marking is not mentioned in the source data, the product complies with the regulatory requirements applicable to Class I devices. Healthcare professionals are invited to scrupulously follow the manufacturer's recommendations to ensure compliant and safe use.


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Manufacturer Hu-Friedy
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