Surgical Tissue Forceps Gerald Perma Sharp 1x2 Straight 18cm - Hu-Friedy
The Pince à tissus Gerald Perma Sharp chirug. 1x2-droite 18cm - 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.
| Manufacturer: Hu-Friedy |
Complete your order
Our customers often order these together
Serrated Gum Scissors - Helmut Zepf (46.050.11TISC) - Delynov
SERAFAST Absorbable Violet Suture 5/0 DS-15 Needle 70cm - Serag & Wiessner - JO103213
Recommended suture
What is the Gerald Perma Sharp tissue forceps?
The Gerald Perma Sharp tissue forceps is a high-end microsurgery instrument developed by the manufacturer Hu-Friedy. This model is distinguished by its straight structure and its 1x2 tip configuration, specifically studied for the manipulation of soft tissues. As a gerald surgical forceps, it is a tool of choice for practitioners demanding fine prehension without compromising tissue integrity. Its design integrates Hu-Friedy's Perma Sharp technology, guaranteeing a finish and durability consistent with the requirements of operating blocks specialized in oral surgery. This instrument belongs to Class I of medical devices.
What are the clinical indications for this instrument?
This gerald surgical forceps is primarily indicated in oral surgery, periodontology, and implantology protocols. It is used for the delicate manipulation of wound edges, the positioning of flaps during complex sutures, or during guided bone regeneration (GBR) procedures. Thanks to its fineness, it allows for intervention in restricted interproximal spaces or on thin tissues where a standard forceps would be too traumatic or bulky. It helps the surgeon stabilize soft tissues to facilitate needle passage during the closure of surgical sites.
What are the technical characteristics of the Hu-Friedy Gerald forceps?
La pince Gerald Perma Sharp présente des spécifications techniques précises pour répondre aux besoins des praticiens en chirurgie orale. Sa longueur totale de 18 cm offre un bras de levier optimal et une excellente visibilité, même en zone postérieure. La partie travaillante est équipée d'un système 1x2 dents (une dent s'insérant entre deux dents opposées), assurant une fixation mécanique stable du tissu prélevé ou déplacé. Cette pince droite est conçue pour résister à des cycles de stérilisation répétés tout en maintenant l'alignement parfait de ses pointes, une caractéristique essentielle pour la microchirurgie.
What are the contraindications for the use of this device?
According to the information provided by Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications mentioned other than inappropriate use by untrained personnel. However, as with any Class I instrument, it is imperative to check the condition of the instrument before each intervention. Use on tissue structures that are too dense or not adapted to the fineness of the 1x2 tips could damage the forceps' teeth or unnecessarily lacerate the patient's tissues.
What are the maintenance precautions for this non-resorbable forceps?
As a reusable metallic surgical instrument, the Gerald Perma Sharp forceps requires a rigorous decontamination and sterilization protocol after each use. Although the specific material is not detailed, Hu-Friedy standards involve thorough cleaning to eliminate organic debris in the 1x2 teeth. It is recommended to scrupulously follow the instructions for use provided by the manufacturer Hu-Friedy 3232 N. Rockwell St. Chicago, Il 60618 USA. Proper maintenance prevents corrosion and guarantees the longevity of the gerald surgical forceps, thus preserving the precision of its grip during successive surgeries.
Who is the manufacturer and what standards are respected?
Le dispositif est fabriqué par Hu-Friedy Mfg. Co., LLC, une entité reconnue mondialement dans le secteur de l'instrumentation chirurgicale orale. Ce produit est classé en Classe I des dispositifs médicaux, conformément à la réglementation en vigueur. Le fabricant est situé au 3232 N. Rockwell St. Chicago, Il 60618 USA. En tant que dispositif de Classe I, il répond aux exigences de sécurité et de performance définies pour cette catégorie d'instruments chirurgicaux manuels. Les praticiens doivent impérativement lire attentivelement la notice d'utilisation avant toute utilisation pour garantir la conformité des soins prodigués avec cet instrument Hu-Friedy.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
