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Surgical Probe Pigtails #2A Handle #31 - Hu-Friedy - Delynov

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The Sonde Pigtail #2A manche #31 - 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.

36.75 € 36.75 EUR 36.75 € Tax Included

36.75 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy Pigtail #2A probe with #31 handle?

The Pigtail #2A probe associated with the #31 handle is a manual diagnostic instrument developed by Hu-Friedy Mfg. Co., LLC. This device consists of a specific working end, known as a pigtail, mounted on an ergonomic #31 type handle. It belongs to the diagnostic instruments category (INSTRU) and is classified as a Class I medical device according to current regulations. Its structure is optimized to offer high tactile sensitivity to the practitioner, allowing for a rigorous evaluation of dental surfaces and surrounding tissues during specialized consultations in oral surgery or periodontics.

What are the clinical indications?

The use of the Hu-Friedy Pigtail #2A probe is indicated for thorough clinical exploration. In oral surgery and implantology, it is used to detect subgingival calculus deposits, evaluate the integrity of prosthetic restorations, and verify the fit of marginal limits. Its curved shape is particularly suitable for probing furcation areas and complex interproximal spaces. It also allows for the diagnosis of surface caries and enamel defects. This instrument is reserved exclusively for qualified healthcare professionals, such as dental surgeons and implantologists, for use in dental practices or hospital environments.

What are the technical characteristics?

The Hu-Friedy #2A probe is distinguished by its Pigtail geometry, characterized by a thin and curved tip that follows anatomical contours. The #31 handle offers a stable grip, essential for maintaining controlled pressure during tissue exploration. As a Class I product manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets standard manufacturing requirements for non-invasive manual instruments. The design prioritizes the transmission of tactile vibrations from the tip to the practitioner's hand, thus facilitating the precise identification of surface irregularities without damaging soft tissues or healthy dental structures.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-Friedy, there are no specific medical contraindications listed for the use of this probe, other than those related to the general use of manual instruments in oral surgery. However, use should be avoided on tissues presenting uncontrolled acute inflammation if the procedure risks exacerbating the pathology without immediate diagnostic benefit. It is imperative to refer to the instructions for use attached to the product to become familiar with the full warnings. Compliance with sterilization protocols is mandatory to prevent any risk of cross-infection between patients.

How is maintenance performed and what are the precautions?

As a non-resorbable and reusable instrument, the Hu-Friedy Pigtail #2A probe requires a rigorous decontamination and sterilization protocol after each intervention. Precautions for use include a systematic visual inspection before each use to check for the absence of deformation or wear of the working tip. A blunt or bent tip could compromise diagnostic accuracy or cause iatrogenic trauma to periodontal tissues. The practitioner must take care not to exert excessive force during probing to preserve the integrity of the instrument and patient comfort. Careful reading of the Hu-Friedy manufacturer's instructions is essential before the first use.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a recognized manufacturer in the dental instrumentation sector for the quality of its manufacturing processes. This product is regulatorily classified as Class I. Although specific CE marking is not mentioned in the source data, the product complies with the regulatory requirements applicable to medical devices in its category. As a Class I instrument, it follows the required conformity assessment procedures to guarantee its safety and performance during normal professional use in a dental or surgical office.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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