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Tissue Forceps Gerald 18cm Surgery 1x2 Curved - Hu-Friedy - Delynov

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The Pince à tissus Gerald 18cm chirug. 1x2-courbée - 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.

75.15 € 75.15 EUR 75.15 € Tax Included

75.15 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy Gerald 18cm tissue forceps?

The Gerald tissue forceps marketed by Delynov is a specialized surgical instrument designed by the manufacturer Hu-Friedy. This model is distinguished by a fine structure and a total length of 18cm, offering an extended reach for deep interventions or in posterior sectors. Its specific configuration features a curved tip equipped with 1x2 teeth jaws, allowing for stable tissue gripping without slipping. Manufactured by Hu-Friedy Mfg. Co., LLC, these forceps are a tool of choice for practitioners demanding precise soft tissue manipulation during rigorous surgical protocols.

What are the clinical indications for these forceps?

This gerald tissue forceps is primarily indicated in oral surgery, periodontology, and implantology. It is used for the delicate manipulation of full-thickness or partial-thickness flaps. Its thinness is particularly suitable during the placement of guided bone regeneration (GBR) membranes or when suturing fine tissues where high placement precision is required. Surgeons also use it to stabilize wound edges during suture needle insertion, thus ensuring precise tissue apposition for optimal healing.

What are the technical characteristics of this instrument?

The technical characteristics of these Hu-Friedy forceps include a length of 18cm, which classifies it among the long instruments in the surgical range. The working part is curved, facilitating access to difficult anatomical areas while maintaining maximum visibility of the operative field. The 1x2 teeth jaw system ensures a light but effective mechanical lock on the tissues, reducing the pressure effort required from the practitioner. As a Class I device, this instrument meets standard manufacturing requirements for non-invasive or short-term invasive manual instrumentation.

What are the contraindications to the use of Gerald forceps?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. Contraindications are not explicitly listed in the short technical documentation, but misuse of the instrument (such as manipulating dense bone or heavy prosthetic material) could damage the thinness of the 1x2 teeth jaws. It is imperative not to use the instrument if it shows signs of corrosion or deformation. The practitioner must systematically refer to the instructions for use before any intervention.

What are the maintenance precautions for this non-resorbable instrument?

As a metallic surgical instrument and not a resorbable device, the Gerald tissue forceps require a rigorous sterilization and cleaning protocol after each use. Although material specifications are not detailed here, Hu-Friedy Class I instruments must be treated according to standard decontamination cycles in an autoclave. The integrity of the 1x2 teeth and the alignment of the curvature should be checked after each cleaning cycle. Particular attention must be paid to drying to avoid any alteration of the instrument's surface over the long term.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This product is classified as a Class I medical device according to current regulations. Hu-Friedy is a globally recognized manufacturer in the dental sector for the quality of its manual instrumentation. Compliance with Class I indicates that the device meets the basic safety and performance criteria for reusable surgical instruments. Professionals must read the instructions carefully to ensure compliance with the maintenance protocols recommended by Hu-Friedy.


State of the art

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

Specifications

Manufacturer Hu-Friedy
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