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Distal Cutting Pliers 0.021 inch x 0.025 inch Non-Retentive - Hu-Friedy - Delynov

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The Pince coupante distale 0.021 inch x 0.025 inch non rétentive - 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.

231.30 € 231.3 EUR 231.30 € Tax Included

231.30 € Tax Included

(0.00 € / Units)
  • Manufacturer

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Instrument

What is the Hu-Friedy 0.021 inch x 0.025 inch distal cutter?

The non-retentive distal cutter developed by Hu-Friedy is a precision instrument intended for sectioning wires and archwires used in orthodontics and maxillofacial surgery. This device is specifically calibrated to handle archwires with dimensions not exceeding 0.021 inch x 0.025 inch. Its non-retentive design means it does not hold the cut fragment after sectioning, requiring careful handling by the practitioner. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the quality requirements of healthcare professionals for procedures requiring a clean and reliable cut of containment or alignment devices.

What are the clinical indications for this non-retentive orthodontic plier?

This non-retentive distal cutter is primarily indicated for extra-oral or intra-oral cutting of orthodontic archwires during corrective treatments or post-surgical stabilization phases. In oral surgery, it is used to adjust fixation devices after GBR or during the placement of containment after orthognathic surgery. It allows for the sectioning of rectangular or round archwires with a maximum capacity of 0.021 x 0.025 inch. Its use is strictly reserved for healthcare professionals trained in dental surgery and orthodontic techniques, ensuring safe integration into the patient care protocol.

What are the technical characteristics of this Hu-Friedy instrument?

The Hu-Friedy non-retentive distal cutter is distinguished by its specific cutting capacity limited to 0.021 inch x 0.025 inch archwires. As a Class I device, it is designed to withstand standard sterilization cycles in clinical environments. Its geometry is optimized to access the distal areas of the dental arch, providing adequate visibility during sectioning. The cutting mechanism is adjusted to minimize manual effort while ensuring a clean section of the metal. Unlike safety models, this non-retentive version leaves the cut segment free, which is often preferred for certain specific removal or adjustment techniques.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is exclusively reserved for qualified healthcare professionals. Contraindications include use on archwires or wires exceeding the technical capacity of 0.021 inch x 0.025 inch, which could damage the cutting jaws or result in an incomplete section. Although the raw MDR text does not list specific patient-related medical contraindications, it is imperative not to use the instrument if it shows signs of wear or corrosion, in order to guarantee the safety of the surgical act and the integrity of the surrounding tissues.

What are the maintenance precautions for this non-absorbable plier?

As a Class I non-absorbable surgical instrument, the Hu-Friedy distal cutter requires a rigorous decontamination and sterilization protocol after each use. The practitioner must carefully follow the instructions for use provided by Hu-Friedy to ensure the longevity of the instrument. Being a non-retentive model, particular precaution must be taken when cutting in the mouth to manually retrieve the sectioned fragment and avoid any ingestion or inhalation by the patient. Regular monitoring of the alignment of the cutting edges is recommended to maintain optimal performance during oral surgery or orthodontic procedures.

Who is the manufacturer and what standards are met by this product?

The 0.021 inch x 0.025 inch distal cutter 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. The manufacturer emphasizes that this instrument is strictly reserved for healthcare professionals. Compliance with Hu-Friedy manufacturing protocols guarantees a reliable tool for the demands of modern dental surgery. Before any use, it is essential to read the accompanying instructions carefully to comply with the manufacturer's specific warnings and maintenance instructions.


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Specifications

Manufacturer Hu-Friedy
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