Tunneling knife #1 short #6 handle
The Couteau de tunnelisation #1 manche #6 court is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the #1 tunneling knife short #6 handle?
The Hu-Friedy #1 tunneling knife short #6 handle is a specialized instrument for gingival surgery. This device belongs to the INSTRU category and is distinguished by its ergonomic configuration adapted to restricted access. Its structure includes a working end specific to model #1, mounted on a short format #6 handle to optimize control during meticulous movements. This Hu-Friedy product is designed to meet the requirements of practitioners performing complex periodontal interventions. As a Class I device, it complies with regulatory standards for reusable surgical instruments, offering a reliable solution for the purchase of a tunneling knife intended for specialized practices.
What are the clinical indications for this surgical tunneling knife?
This #1 tunneling knife is primarily indicated for gingival and periodontal surgery. Its use is recommended in tunneling techniques aimed at treating tissue recessions. It allows for the preparation of the recipient site for the insertion of connective tissue grafts or collagen matrices without resorting to relaxing incisions. Gum surgery instrumentation of this type is essential for preserving collateral vascularization and the integrity of the interdental papillae. Using this Hu-Friedy instrument facilitates precise mucoperiosteal detachment, ensuring optimal preparation of the tunnel before positioning the filling material or the autologous graft.
What are the technical characteristics of this instrument?
The Hu-Friedy #1 tunneling knife features specific technical characteristics for micro-surgery. It is equipped with a short #6 handle, a dimension designed to improve maneuverability in the posterior area or in patients with limited mouth opening. The #1 working part has a sharpened geometry to allow for atraumatic dissection of periodontal tissues. This device is classified as a Class I instrument according to current regulations. The design by the manufacturer Hu-friedy ensures compliance with manufacturing requirements for professional medical devices. Its design is optimized for gingival surgery procedures requiring great finesse in execution.
What are the contraindications for the use of this gum tunneling knife?
The use of this surgical tunneling knife is strictly reserved for healthcare professionals qualified in oral and periodontal surgery. Although the raw regulatory text does not list specific medical contraindications related to patient pathology, use is contraindicated for any person not possessing the required clinical training. It is necessary to systematically refer to the instructions for use provided by the manufacturer Hu-friedy to identify any restrictions related to the state of the patient's tissues or allergies to standard metallic components of surgical instruments. Compliance with sterilization protocols is imperative before any intervention.
What are the maintenance precautions for this non-resorbable instrument?
As a Class I reusable surgical instrument, the #1 tunneling knife short #6 handle requires a rigorous decontamination and sterilization protocol after each use. Although material specifications are not detailed, this type of gum surgery instrumentation must be treated according to the instructions of the manufacturer Hu-friedy located in Chicago, USA. Practitioners must inspect the sharpness of the #1 blade before each intervention to guarantee the effectiveness of the surgical movement. Careful handling is required to avoid any deformation of the working end. It is recommended to follow the recommended cleaning cycles to maintain the integrity of the short #6 handle and the longevity of the Hu-Friedy instrument.
Who is the manufacturer and what standards are respected?
The #1 tunneling knife is manufactured by Hu-friedy, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed under Class I, which attests to its compliance with basic regulatory requirements for non-invasive or transiently invasive surgical instruments. The manufacturer specifies that this product is exclusively reserved for healthcare professionals. Before any use, it is imperative to read the provided instructions carefully to ensure compliance with warnings and safety procedures. The traceability and manufacturing quality of the Hu-Friedy guarantee a tool adapted to the standards of modern oral surgery.
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Specifications
| Manufacturer | Hu-Friedy |
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