Instrument for sinus lift urban number 1 (short handle S6) - Hu-Friedy - [impurba1s6] - Delynov
The Instrument à Sinus Lift Urban #1 manche #6 court- 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: IMPURBA1S6.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Hu-Friedy |
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What is the Urban #1 Sinus Lift Instrument with #6 short handle?
The Urban #1 Sinus Lift instrument, referenced under code IMPURBA1S6 by Hu-Friedy, is a specialized manual device for oral surgery. Its structure consists of a working part specific to the Urban technique and a #6 short type handle. This compact design is intended to offer better ergonomics in reduced clinical spaces. Manufactured by Hu-Friedy Mfg. Co., LLC, this Class I device is a non-resorbable metallic tool intended for use during critical phases of sinus floor augmentation. The Hu-Friedy brand ensures rigorous manufacturing to meet the requirements of dental surgeons and implantologists.
What are the clinical indications for this elevator?
This membrane elevator is primarily indicated during pre-implant surgeries, specifically for sinus lift (sinus elevation) via a lateral approach. It is used after the osteotomy of the lateral wall of the maxillary sinus. Its function is to separate the sinus membrane from the bone without causing perforation. The use of a short Urban elevator is particularly relevant in patients with limited mouth opening or during interventions in posterior sectors where the standard length of instruments can hinder the surgical gesture. It allows for precise manipulation to prepare the site before the introduction of bone substitutes.
What are the technical characteristics of the IMPURBA1S6 instrument?
The IMPURBA1S6 instrument is distinguished by its Urban #1 configuration coupled with a #6 short handle. Unlike standard handles, this short version reduces the overall bulk of the tool, offering better tactile control and a reduction in unwanted leverage in difficult-to-access areas. The working part is designed to follow the anatomical contours of the sinus cavity. As a Hu-Friedy product, it benefits from the manufacturer's expertise in metal treatment to guarantee longevity and resistance to repeated sterilization. This device belongs to Class I of medical devices.
What are the contraindications for the use of this instrument?
According to data from the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed for this instrument other than those related to the sinus lift surgical procedures themselves. General contraindications include acute sinus pathologies, untreated local infections, or systemic contraindications to implant surgery. The use of this instrument is strictly reserved for qualified healthcare professionals. It is imperative to read the instructions carefully before use to ensure the device's suitability with the patient's clinical state and the absence of known allergies to the metallic components of the device.
What are the maintenance and storage precautions?
As a non-resorbable metal instrument, this Hu-Friedy device requires a rigorous decontamination, cleaning, and sterilization protocol after each use. Practitioners must ensure they do not use corrosive cleaning agents that could alter the surface condition of the steel. Being a Class I instrument, its maintenance must follow standard recommendations for reusable surgical devices. A visual inspection of the working part of the sinus lift elevator is recommended before each intervention to detect any wear or deformation that could compromise the safety of the sinus membrane during detachment.
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. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its surgical instruments. This product is classified as a Class I medical device. It is essential that the user verifies local regulatory compliance before purchasing on Delynov. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument meets safety requirements for professional use in a surgical environment. The instructions for use provided by the manufacturer must be systematically consulted to ensure usage compliant with standards of care.
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