Fragment Forceps Steiglitz 45 Degrees 13.5 cm - Hu-Friedy - Delynov

What is the Hu-Friedy Steiglitz 45° 13.5 cm fragment forceps?

The Steiglitz 45° 13.5 cm fragment forceps is a high-precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. It belongs to the category of Guided Bone Regeneration (GBR) and oral surgery devices. Its structure is characterized by a working part angled at 45 degrees, mounted on a 13.5 cm body. This device is specifically designed to provide a firm and secure grip on small elements that are difficult to grasp with standard instruments. As a Class I medical device, it meets regulatory requirements for use in professional clinical environments. Its design by Hu-Friedy guarantees a reliable instrument for daily oral surgery procedures.

What are the clinical indications for these dental fragment forceps?

These dental fragment forceps are primarily indicated for root extraction and debris removal during alveolar surgeries. They are particularly useful for recovering fractured root fragments, apices, or small bone sequestra. The use of the steiglitz 45 forceps is recommended when direct access is limited by the patient's anatomy or the position of the tooth. It is effective in complex avulsion protocols where an angled steiglitz forceps is necessary to bypass anatomical obstacles without compromising the visibility of the surgical field. Its use is strictly reserved for qualified healthcare professionals practicing dental surgery, implantology, or maxillofacial surgery.

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

The Steiglitz fragment forceps from Hu-Friedy features precise technical specifications to meet the needs of practitioners. It has a total length of 13.5 cm, offering an ideal balance between leverage and maneuverability. Its 45-degree angulation at the jaws allows for a tangential or angled approach, essential for reaching the bottom of sockets. The thinness of its tips is designed to fit into restricted spaces without damaging surrounding tissues. This Hu-Friedy device is classified as Class I according to medical device regulations. The manufacturing quality of Hu-Friedy Mfg. Co., LLC ensures mechanical resistance adapted to the stresses of gripping hard mineralized tissues such as dentin or bone.

What are the contraindications for using the root extraction forceps?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond the intended use. However, the use of these root extraction forceps is strictly reserved for trained healthcare professionals. The instrument should not be used for tasks for which it is not intended, such as handling heavy prosthetic materials that could damage the thinness of the 45-degree jaws. Practitioners must systematically refer to the instructions for use before any intervention. Compliance with sterilization and maintenance protocols is imperative to guarantee patient safety and the integrity of the instrument during surgical procedures.

What are the precautions for use and maintenance for this Class I device?

Being a Class I medical device, the angled steiglitz forceps requires rigorous management by healthcare personnel. Before the first use and after each surgical act, the instrument must be cleaned, disinfected, and sterilized in accordance with the instructions from the manufacturer Hu-Friedy. It is crucial to visually inspect the alignment of the jaws and the condition of the joint to maintain optimal gripping force. Although details on the composition are not specified, this type of surgical instrumentation requires complete drying to avoid any corrosion. Handling must be precise so as not to deform the 45-degree angulation, thus ensuring the longevity of the tool in the dental office's surgical arsenal.

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

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 for the quality of its dental surgery instrumentation. This product is listed as a Class I medical device. The manufacturer emphasizes that the use of these fragment forceps is exclusively reserved for healthcare professionals. Users are invited to read the instructions carefully before any use to ensure compliance with safety and clinical efficacy standards. Traceability and compliance with manufacturer directives ensure safe use for the patient and the practitioner during oral surgery interventions.

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