Sinus Lift Elevator Curette Simion No.1 3.5mm Handle No.6 - Hu-Friedy (PESIM16) - Delynov
The Curette élévat. sinus Simion #1 3,5mm manche #6 - 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 Simion #1 sinus elevat. curette 3.5mm handle #6 - Hu-Friedy?
The Simion #1 sinus elevat. curette from the brand Hu-Friedy is a manual surgical instrument specifically developed for oral and implant surgery. This device consists of an active part with a 3.5mm diameter mounted on a #6 handle, offering a grip adapted to the requirements of micro-surgery. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument is designed to delicately manipulate soft tissues within the sinus cavity. As a Class I medical device, it meets the rigorous manufacturing standards of a manufacturer recognized worldwide for the quality of its stainless steel instrumentation. Its structure is optimized to guarantee precise tactile transmission during the procedure.
What are the clinical indications for this instrument?
The use of this sinus elevation curette is mainly indicated during sinus lift or sinus elevation procedures. It is used after the osteotomy of the lateral sinus wall to initiate and finalize the detachment of the Schneiderian membrane from the internal bony wall. Its design allows access to the sinus recesses to release the membrane without perforation, a crucial step before the insertion of a bone substitute. It is used by dental surgeons and implantologists as part of prosthetic rehabilitations requiring an increase in sub-sinus bone height. The instrument is exclusively reserved for healthcare professionals trained in these advanced surgical techniques.
What are the technical characteristics of the Simion #1 curette?
The Simion #1 sinus elevator curette is distinguished by a 3.5mm working end, sized to offer a balance between visibility and detachment efficiency. The Hu-Friedy #6 handle is a large-diameter handle, designed to reduce manual fatigue for the practitioner during prolonged procedures while maintaining optimal control. The instrument is classified as Class I according to medical device regulations. The surface finish and assembly quality guarantee resistance to repeated autoclave sterilization cycles. Every technical detail, from the curvature of the shank to the profile of the curette, is designed to match the internal anatomy of the maxillary sinus.
What are the contraindications for the use of this device?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, contraindications are related to the intended use and general warnings of surgical practice. The use of this instrument is prohibited for any unqualified personnel, as it is strictly reserved for healthcare professionals. Although the raw MDR text does not list specific biological contraindications, clinical caution dictates not using the instrument in cases of untreated acute sinus infection or in patients with systemic pathologies contraindicating sinus lift surgery. It is imperative to read the instructions carefully and respect asepsis protocols before any intervention.
What are the maintenance precautions for this non-resorbable curette?
As a non-resorbable metallic instrument, the sinus lift curette requires a rigorous decontamination and sterilization protocol after each use. Precautions include immediate pre-disinfectant cleaning to avoid the fixation of organic residues, followed by ultrasonic or manual cleaning with neutral pH solutions. Drying must be meticulous before autoclaving to prevent any corrosion. Hu-Friedy recommends following the specific reprocessing instructions to preserve the integrity of the steel and the precision of the 3.5mm active part. Regular visual examination of the condition of the #6 handle and the tip is advised to guarantee patient safety and the effectiveness of the surgical movement.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I, which implies compliance with the safety and performance requirements applicable to this category of reusable surgical instruments. Although specific CE marking is not mentioned in the source data, manufacturing by Hu-Friedy ensures compliance with high industrial quality standards. Healthcare professionals should refer to the labeling and instructions for use to confirm application procedures and safety warnings. Delynov ensures the distribution of this precision instrument for clinics specialized in implantology.
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Specifications
| Manufacturer | Hu-Friedy |
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