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Dental Surgery Instrument Set - Brewer - Hu-Friedy - Delynov.

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The Pince porte crampon - 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.

165.15 € 165.15 EUR 165.15 € Tax Included

165.15 € Tax Included

(0.00 € / Units)
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Instrument

What is the rubber dam clamp forceps - Hu-Friedy - Delynov?

The dental rubber dam clamp forceps developed by Hu-Friedy is a specific manual instrument designed for handling rubber dam clamps. This Class I medical device, manufactured by Hu-Friedy Mfg. Co., LLC, features an articulated structure allowing the clamp springs to be spread in order to position them around the neck of the teeth. Its design meets the requirements of clinical practice in dentistry and oral surgery, offering a reliable interface between the practitioner's hand and the isolation accessory. As a product from a recognized manufacturer, this instrument is intended for rigorous use in dental offices to guarantee the sealing of the operative field.

What are the clinical indications for this instrument?

The use of the rubber dam clamp forceps is indicated during any intervention requiring the placement of a rubber dam for the isolation of the surgical site. It is primarily used in endodontics, restorative dentistry, and during certain phases of oral surgery or GBR (Guided Bone Regeneration) where a dry and decontaminated environment is required. The instrument allows for grasping the clamp, widening it through manual pressure, and then releasing it with precision onto the target tooth. This action is fundamental for maintaining the dam in place and protecting the patient's soft tissues and airways during treatment.

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

The Hu-Friedy rubber dam clamp forceps is distinguished by ergonomics adapted to the hands of healthcare professionals, allowing for controlled force transmission to open clamps, even the most rigid ones. Although composition specifications are not detailed in the source data, manufacturing by Hu-Friedy Mfg. Co., LLC guarantees an instrument compliant with Class I standards. The locking or sliding mechanism, typical of these forceps, ensures that the clamp remains in an open position without excessive effort from the practitioner, thereby reducing muscle fatigue during complex operative field placements.

What are the contraindications for the use of this instrument?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed, other than the fact that use is strictly reserved for qualified healthcare professionals. The use of the rubber dam forceps should be avoided if the instrument shows signs of wear or deformation that could compromise the hold on the clamp, which could lead to trauma of the periodontal tissues or accidental ingestion of the accessory. It is necessary to systematically refer to the technical manual and manufacturer warnings located at 3232 N. Rockwell St. Chicago, Il 60618 USA before any clinical handling.

What are the maintenance and durability precautions?

As a non-resorbable Class I instrument, the rubber dam clamp forceps requires a rigorous sterilization and cleaning protocol after each use, in accordance with Hu-Friedy guidelines. Healthcare professionals must regularly inspect the jaws of the forceps to ensure they insert correctly into the clamp perforations. Periodic lubrication of the joint may be necessary to maintain smooth movement. Compliance with the decontamination cycles recommended by the manufacturer ensures the longevity of the instrument and prevents risks of cross-corrosion within the dental surgery technical tray.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, USA. This product is classified as a Class I medical device according to current regulations. Although specific CE marking is not mentioned in the current technical sheet, the product complies with regulatory requirements applicable to manual dental instruments in the United States and international markets where the brand is distributed. As a device reserved for healthcare professionals, it must be used according to the indications and warnings provided by Hu-Friedy to ensure patient safety and the effectiveness of the surgical procedure.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Hu-Friedy
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