Hemostatic Forceps Kelly No. 2 14cm Curved - Hu-Friedy - Delynov
The Pince hémostatique Kelly #2 14cm 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.
What is the Hu-Friedy Kelly #2 14cm curved hemostatic forceps?
The Kelly #2 hemostatic forceps developed by Hu-Friedy is a metallic surgical instrument designed for oral and maxillofacial surgery. This device is distinguished by its hinged structure and curved jaws, allowing for a firm and secure grip. With a total length of 14 cm, this instrument is specifically calibrated to meet the requirements of the oral space, offering the practitioner optimal control during clamping phases. Manufactured by Hu-Friedy Mfg. Co., LLC, these forceps are a standard tool for soft tissue management and temporary hemostasis in clinical settings.
What are the clinical indications for this instrument?
In oral, implant, and periodontal surgery, the Kelly #2 forceps is primarily indicated for hemostasis by compression of small-caliber vessels. It is also used for grasping and manipulating soft tissues, membranes during guided bone regeneration (GBR) procedures, or for the removal of small tissue fragments. Its curvature is a major asset for navigating around complex anatomical structures and maintaining clear visibility of the surgical site, thus facilitating technical maneuvers in difficult-to-access sectors.
What are the technical characteristics of the Kelly #2 forceps?
The main technical characteristics of this Hu-Friedy instrument include a length of 14 cm, ideal for balanced handling. The working part features curved jaws, which allow for the application of distributed gripping force while following the natural curves of oral tissues. The ratchet locking mechanism allows for constant pressure to be maintained without continuous effort from the surgeon's hand. This device belongs to the Class I instrument category, guaranteeing its compliance with manufacturing standards for non-invasive or short-term invasive medical devices.
What are the contraindications for the use of these forceps?
Specific contraindications are not explicitly detailed in the technical documentation provided by the manufacturer Hu-Friedy Mfg. Co., LLC, beyond standard surgical protocols. However, the use of this instrument is strictly reserved for qualified healthcare professionals. The instrument should not be used for unintended tasks, such as manipulating rigid materials that could damage the jaws, or on patients with known sensitivities to the alloy components, although not specified here. A review of the instructions before use is imperative.
What are the maintenance and durability precautions?
As a non-resorbable and reusable instrument, the Kelly #2 forceps requires a strict cleaning, disinfection, and sterilization protocol between each patient. To preserve the integrity of the hinge mechanism and the efficiency of the ratchet, it is recommended to follow the cleaning instructions from the manufacturer Hu-Friedy. Particular attention must be paid to drying to prevent any corrosion. Although the instrument is robust, regular inspection of the curved jaws is necessary to ensure the absence of deformation, thus guaranteeing consistent performance during dental surgery procedures.
Who is the manufacturer and what standards are met?
The Kelly #2 hemostatic forceps is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St., Chicago, USA. This medical device is classified as Class I according to current regulations. As a recognized manufacturer in the dental sector, Hu-Friedy adheres to rigorous production standards to ensure the reliability of its surgical instruments. The product is intended exclusively for professional use. Practitioners must imperatively read the instructions for use and warnings provided by the manufacturer carefully to ensure use in accordance with patient safety standards.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Hu-Friedy |
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