Tissue Grasping Forceps Cooley Micro Straight Sinusl Handle 18cm Mod - Hu-Friedy - Delynov
The Pince à tissus Micro Cooley manche SinusL 18cm droite mod- Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.
- Compliance: Medical device Class I.
- Manufacturer: Hu-Friedy Mfg. Co., LLC.
- Reference: TPSLCOSM.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Hu-Friedy micro cooley forceps?
The micro cooley forceps from the Hu-Friedy brand is a specialized instrument designed for microsurgery and guided bone regeneration. This specific model, referenced under code TPSLCOSM, is distinguished by its SinusL handle and its modified straight configuration. Manufactured by Hu-Friedy Mfg. Co., LLC, this micro surgical forceps is intended for practitioners requiring high precision when handling soft tissues. Its structure is optimized to offer superior tactile control, essential during delicate interventions in implantology or periodontology where maintaining tissue integrity is critical.
What are the clinical indications for this instrument?
This instrument is primarily indicated for complex oral surgery interventions, notably during sinus lift or guided bone regeneration (GBR) procedures. The cooley micro surgery forceps allows for the stabilization of soft tissue flaps or the precise positioning of collagen membranes. Its use is particularly relevant in difficult-to-access areas where standard instruments lack finesse. It assists the dental surgeon or implantologist during suturing stages and the manipulation of fine tissues, ensuring a micro-surgical approach that respects the surrounding anatomical structures.
What are the technical characteristics of the TPSLCOSM forceps?
The Hu-Friedy sinus micro surgery forceps features precise technical characteristics to meet clinical constraints. It has a total length of 18cm, allowing it to reach posterior sectors without visual obstruction. The SinusL handle is specially designed to provide a stable grip while reducing fatigue during prolonged interventions. The working part is a modified straight tip, characteristic of the micro-surgery cooley range, offering a gripping surface adapted to fragile tissues. This device is classified as a Class I instrument according to current regulatory standards.
What are the contraindications for using this forceps?
According to data provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed for this instrument outside of standard oral surgery protocols. However, the use of this tissue microsurgery forceps is strictly reserved for qualified healthcare professionals. It is imperative not to use the instrument for tasks for which it is not intended, such as manipulating rigid materials or dense bone, which could damage the finesse of the Cooley tip and compromise its precision during subsequent uses on soft tissues.
What are the maintenance precautions for this non-resorbable instrument?
As a reusable metallic surgical instrument of Class I, the micro-surgery cooley forceps requires a rigorous sterilization protocol between each patient. Although composition details are not specified, the maintenance of Hu-Friedy instrumentation generally follows ultrasonic cleaning, rinsing, and autoclave sterilization procedures. Practitioners must carefully read the instructions before use to respect the sterilization cycles recommended by the manufacturer. Particular attention must be paid to the inspection of the modified straight tip to ensure the absence of residues or deformations before any new intervention.
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. As a Class I instrument, it meets the safety and performance requirements applicable to medical devices in this category. The Hu-Friedy brand is globally recognized for the quality of its dental surgery instrumentation. The product is distributed by Delynov and must be used in accordance with the manufacturer's instructions. Compliance with Class I ensures that the instrument has undergone the necessary conformity assessments for its use in a professional clinical environment.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Hu-Friedy |
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