Instrument for sinus lift Urban number 2 (long handle) - Hu-Friedy - [IMPURBAN26] - Delynov
The Instrument pour Sinus Lift Urban #2 - 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.
What is the Urban #2 Sinus Lift instrument - Hu-Friedy?
The Urban #2 Sinus Lift instrument, designed by the manufacturer Hu-Friedy, is a specialized surgical tool intended for sinus floor augmentation interventions. This manual device is part of the high-precision instrumentation range developed by Hu-Friedy Mfg. Co., LLC for implant surgery. Its structure is optimized for handling delicate tissues within the sinus cavity. As a Class I medical device, it meets the basic regulatory requirements for use in a clinical setting by trained practitioners. Its design allows for rigorous handling during the critical phases of sub-sinus access.
What are the clinical indications for this instrument?
The Urban #2 instrument is primarily indicated in pre-implant surgery protocols, specifically during a lateral approach sinus lift. Its role is central as a sinus membrane elevator, allowing for the careful separation of the Schneiderian membrane from the internal bony wall of the maxillary sinus. This step is essential to release a sufficient volume intended to receive a bone graft or a bone substitute. It is used by dental surgeons, stomatologists, and implantologists during complex maxillary rehabilitations where the residual bone volume is insufficient for immediate implant placement.
What are the technical characteristics of the Urban #2 instrument?
The Urban #2 instrument from the Hu-Friedy brand features specific geometric characteristics adapted to the anatomy of the maxillary sinus. Although the precise materials are not detailed in the provided technical documentation, the manufacturing standards of Hu-Friedy Mfg. Co., LLC guarantee a tool suitable for sterilization and repeated use in the operating room. Its shape is designed to offer optimal angulation, facilitating passage through the lateral bony window and allowing access to the peripheral areas of the membrane without exerting excessive pressure. This Class I device is a key element of the instrumentation for soft and hard tissue management in implantology.
What are the contraindications for the use of this device?
According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. General contraindications include any clinical situation where sinus lift surgery is proscribed, such as acute sinus infections, local tumor pathologies, or general medical contraindications to oral surgery. It is imperative to refer to the instructions for use and warnings provided by Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA before any intervention. The practitioner must evaluate the benefit/risk ratio for each patient, particularly in cases of extreme fragility of the sinus mucosa.
What are the precautions for use and maintenance?
As a non-resorbable and reusable instrument, the Urban #2 requires a rigorous decontamination and sterilization protocol between each patient, in accordance with Hu-Friedy's instructions. The practitioner must inspect the instrument before each use to ensure the absence of deformation or damage to the working parts. Particular attention must be paid when using it as a membrane elevator to avoid any accidental perforation of the Schneiderian membrane. Handling must be precise and fluid. Compliance with the cleaning cycles recommended by the manufacturer Hu-Friedy Mfg. Co., LLC is essential to maintain the functional integrity of the device over the long term.
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 manufacturer is globally recognized for the quality of its surgical instrumentation. The product is classified as a Class I medical device. It is essential to read the instructions carefully and respect the manufacturer's warnings before any use. Compliance with Class I standards ensures that the device meets the safety and performance requirements defined for this category of manual instruments. Any use must be carried out by a healthcare professional competent in the field of implant and oral surgery.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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