Instrument for Sinus Lift Urban Number 2 Handle (Short Handle S6) - Hu-Friedy - [IMPURBA2S6] - Delynov

What is the Urban #2 sinus lift instrument with short #6 handle?

The Urban #2 sinus lift instrument is an oral surgery device developed by Hu-Friedy, a recognized manufacturer in the field of medical instrumentation. This urban instrument is distinguished by its specific configuration including a short #6 handle, optimizing grip and control during critical phases of the intervention. Its structure is designed to meet the requirements of practitioners performing sinus elevations, where precision of movement is paramount to preserve the integrity of soft tissues. This short sinus lift elevator is part of the specialized range from Hu-Friedy Mfg. Co., LLC, guaranteeing a manufacturing quality compliant with industry standards for Class I devices.

What are the clinical indications for this instrument?

This instrument is primarily indicated for implant and oral surgery procedures requiring an elevation of the sinus floor. As an urban elevator, it is used after the osteotomy to gently separate the Schneiderian membrane from the underlying bone wall. The use of this short sinus elevator is particularly relevant during lateral approach procedures or in clinical situations where the workspace is limited by the patient's anatomy. It allows for the creation of the space necessary for the insertion of bone grafting material. Its use is strictly reserved for qualified healthcare professionals, as specified by the manufacturer Hu-Friedy in the instructions for use.

What are the technical characteristics of the IMPURBA2S6 instrument?

The instrument referenced under code IMPURBA2S6 by Hu-Friedy features technical characteristics focused on maneuverability. Its specificity lies in its short #6 handle, an ergonomic variant that reduces the overall bulk of the tool compared to standard handles. This feature is essential for interventions in the posterior zone where the patient's mouth opening may limit the passage of long instruments. The Urban #2 working part is calibrated to offer an optimal balance between finesse and resistance, allowing for atraumatic dissection of the sinus membrane. As a Class I device, it meets the basic regulatory requirements for reusable surgical instruments, requiring a rigorous sterilization protocol before each use.

What are the contraindications for the use of this instrument?

The contraindications related to the use of this short sinus lift instrument are primarily dictated by the patient's clinical condition and oral surgery protocols. Although the raw MDR text does not list specific medical contraindications such as metal allergies, it is imperative that the practitioner evaluates the feasibility of the procedure based on the patient's systemic health (coagulation disorders, active sinus pathologies, etc.). The use of this instrument is contraindicated for any person who does not have the qualification of a healthcare professional. Failure to comply with cleaning and sterilization protocols also constitutes a major contraindication to its use in a clinical setting to avoid any risk of cross-contamination.

What are the maintenance precautions for this non-resorbable instrument?

As this is a reusable metallic surgical instrument and not a resorbable device, precautions relate exclusively to its life cycle and maintenance. The Urban #2 sinus lift instrument must be cleaned, disinfected, and sterilized before its first use and after each surgical intervention, in accordance with the instructions provided by Hu-Friedy. It is crucial to follow the manufacturer's recommendations regarding cleaning agents to avoid any corrosion or degradation of the short #6 handle. The practitioner must regularly inspect the condition of the working ends to ensure the absence of deformations or premature wear that could compromise safety during the detachment of the sinus membrane. Storage in a dry and clean environment is essential.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device belongs to Class I according to the regulatory classification of medical devices. Hu-Friedy is a manufacturer recognized worldwide for the rigor of its production processes and the quality of its surgical steels. Although the specific CE marking is not detailed in the source data, the product complies with American and international manufacturing standards for instruments in its category. Users are invited to read the instructions for use carefully before any handling. Traceability and compliance with Class I standards ensure that the instrument meets the safety and performance requirements for use in implant surgery.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.