Peet 45 Degree 12cm Fragment Forceps for Dental Surgery - Hu-Friedy - Delynov

What is the Peet 45° 12cm fragment forceps - Hu-Friedy?

The Peet 45° 12cm fragment forceps is an oral surgery instrument designed by the manufacturer Hu-Friedy. This Peet forceps is distinguished by its specific structure including a working part angled at 45 degrees and a total length of 12cm. It is primarily used for handling small elements during surgical interventions. As a precision instrument, it allows practitioners to firmly grasp small objects in a restricted operative environment. Its design by Hu-Friedy Mfg. Co., LLC guarantees a tool adapted to the requirements of dental and maxillofacial surgery operating blocks.

What are the clinical indications for this dental Peet forceps?

The clinical indications for this dental fragment forceps primarily concern oral surgery and guided bone regeneration (GBR) procedures. It is indicated for the extraction of root fragments, the removal of bone splinters after alveoloplasty, or the handling of small debris during complex surgical acts. Its Peet forceps shape with a 45-degree angulation makes it particularly useful for reaching difficult-to-access areas, such as posterior sectors, where a straight forceps would not allow optimal visibility or grip. It is exclusively reserved for use by qualified healthcare professionals.

What are the technical characteristics of this instrument?

The Peet 45° 12cm fragment forceps presents precise technical characteristics to meet the needs of implantology and oral surgery. It measures exactly 12cm in length, thus offering maneuverability adapted to fine movements. The distinctive element is its 45° inclination at the level of the jaws, which facilitates passage over anatomical or prosthetic obstacles. Manufactured by Hu-Friedy, this surgical ENT forceps benefits from the expertise of a manufacturer recognized for the quality of its instruments. It belongs to the category of Class I devices according to current regulations, ensuring its compliance for use in dental practices or hospital settings.

What are the contraindications for the use of the root fragment forceps?

In accordance with the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond the intended use. However, the use of this instrument is strictly reserved for trained healthcare professionals. Standard sterilization and maintenance protocols for Class I devices must be followed to avoid any risk of cross-contamination. The instrument must not be used for tasks for which it was not designed, such as handling excessively hard materials that could damage the adjustment of the 45-degree jaws.

What are the precautions for use for this Peet forceps?

To guarantee the longevity of the Hu-Friedy dental Peet forceps, several precautions must be observed. Before the first use and after each intervention, it is imperative to carefully read the manual and follow the manufacturer's cleaning and sterilization instructions. Although this instrument is not a resorbable device, its durability depends on compliance with decontamination cycles. The practitioner must check the alignment of the jaws and the absence of corrosion before each act. Being a Class I device, its regular maintenance is essential to maintain the precision of fragment gripping during GBR surgeries or extractions.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a globally recognized manufacturer in the dental sector for the quality of its instrumentation. This product is classified as a Class I medical device. Compliance with this classification guarantees that the instrument meets the safety and performance requirements defined for non-invasive or reusable surgical tools of this type. Healthcare professionals must ensure the authenticity of the instrument by checking the manufacturer's markings on the body of the 12cm forceps.

State of the art

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