Surgical Fine Curved Fabric Forceps 1x2 14.5cm - Hu-Friedy - Delynov
The Pince à tissus chirug.-fine courbée 1x2 14,5cm - 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 surg.-fine curved 1x2 14.5cm tissue forceps?
The Hu-Friedy surg.-fine curved 1x2 14.5cm tissue forceps is a precision instrument intended for the manipulation of soft tissues in oral surgery. It is distinguished by its fine ends equipped with 1x2 type teeth, allowing for a secure grip of flaps. Its curved shape is specifically designed to provide increased visibility and simplified access to complex surgical sites. Manufactured by Hu-Friedy Mfg. Co., LLC, these fine surgical forceps meet the requirements of practitioners seeking a reliable tool for the critical stages of surgical exposure and wound closure. Its robust structure guarantees a faithful transmission of the force exerted by the surgeon.
What are the clinical indications for these curved tissue forceps?
These curved tissue forceps are primarily indicated in oral surgery procedures, particularly during Guided Bone Regeneration (GBR) and periodontology techniques. They are used to grasp, lift, and hold gingival tissues or membranes during the placement of grafts or filling materials. Their use is essential for stabilizing incision margins during the passage of suture needles, thus ensuring precise tissue coaptation. As an instrument reserved for healthcare professionals, it finds its utility in all interventions requiring atraumatic but firm manipulation of soft structures, thus minimizing the risks of tissue tearing during repeated manipulations.
What are the technical characteristics of this instrument?
The forceps are characterized by a total length of 14.5cm, offering an ideal balance between maneuverability and reach. The working part is equipped with a 1x2 teeth system, meaning one tooth fits between two others for effective mechanical locking of the tissue. Its fine curvature allows for bypassing anatomical obstacles, such as adjacent teeth, without obstructing the practitioner's visual field. This Hu-Friedy device is classified as a Class I instrument according to current regulations. Its ergonomic design allows for a stable grip, reducing fatigue during prolonged interventions. It is specifically adapted to the requirements of micro-surgery and modern implant surgery.
What are the contraindications for the use of this device?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed other than inappropriate use by untrained personnel or for applications not intended by the manufacturer. Practitioners must refer to the instructions for use to ensure that the instrument is used in accordance with oral surgery protocols. As with any surgical instrument, a preliminary inspection is necessary to check the integrity of the teeth and the joint before each intervention to avoid any intraoperative incident related to excessive wear or structural damage.
What are the maintenance precautions for these non-absorbable forceps?
Although the term absorption applies to sutures, the longevity of these non-absorbable fine surgical forceps depends on rigorous sterilization protocols. As a Class I device, it must be cleaned, disinfected, and sterilized before each use according to the manufacturer Hu-Friedy's instructions. It is crucial to follow autoclave recommendations to preserve the mechanical properties of the steel and the alignment of the 1x2 teeth. Particular attention must be paid to cleaning the gripping areas and the joint to eliminate any biological residue. Proper maintenance ensures not only patient safety but also extends the operational life of the instrument in the dental office.
Who is the manufacturer and what standards are respected?
The device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a manufacturer recognized worldwide for the quality and precision of its surgical instruments. This product is listed under Class I, which attests to its compliance with the basic regulatory requirements for medical devices in this category. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Before any use, it is imperative to carefully read the provided manual to respect the warnings and conditions of use defined by Hu-Friedy, thus guaranteeing a safe and effective surgical practice.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Hu-Friedy |
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