Novatech #12 cement remover #2 handle - Hu-Friedy - Delynov
The Enlève ciment Novatech #12 manche #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 Novatech #12 cement remover handle #2?
The Novatech #12 cement remover handle #2 is a precision manual instrument designed by Hu-Friedy, a recognized manufacturer in dental instrumentation. This device is specifically structured for post-cementation cleaning tasks. It consists of a Novatech #12 working part mounted on a #2 type handle, providing a configuration adapted to the requirements of oral surgery. This dental cement removal instrument is designed to meet the needs of practitioners requiring constant reliability during prosthetic finishing phases. As a Class I device, it complies with the rigorous quality standards of Hu-Friedy Mfg. Co., LLC, guaranteeing safe professional use within the dental practice.
What are the clinical indications for this instrument?
The intended use of this instrument primarily concerns the removal of cement residues after the placement of crowns, bridges, or implant abutments. In oral surgery and implantology, the accumulation of luting materials can lead to periodontal or peri-implant complications if not correctly eliminated. This cement scraping instrument is therefore indicated for sanitizing cervical and interproximal areas. Its application helps maintain the integrity of soft tissues by eliminating chemical or mechanical irritants. Use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-Friedy located in Chicago, USA.
What are the technical characteristics of this instrument?
The Hu-Friedy instrument is distinguished by its Novatech #12 configuration, a geometry specifically studied for access to posterior areas. The #2 handle offers a grip adapted to the precision maneuvers necessary for the dental cement scaler. Although the exact material composition is not specified in the source data, manufacturing by Hu-Friedy Mfg. Co., LLC ensures compliance with the requirements for Class I medical devices. The architecture of the instrument is designed to withstand standard cleaning and sterilization cycles in a clinical environment, while maintaining the effectiveness of its working part for clean removal of excess cement.
What are the contraindications for the use of this cement remover?
According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is exclusively reserved for healthcare professionals. Specific contraindications are not detailed in the raw technical documentation, but use must strictly comply with the clinical indications for cement removal. It is the practitioner's responsibility to evaluate potential risks based on the patient's clinical status, particularly in cases of fragile prosthetic structures or hypersensitive gingival tissues. It is imperative to read the instructions carefully before use to ensure that the device is employed according to the safety protocols established by Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA.
What are the precautions for use and maintenance?
As a non-resorbable instrument intended for repeated use, this dental cement remover requires a rigorous maintenance protocol. The practitioner must ensure systematic cleaning after each intervention to eliminate cement debris that could set on the Novatech working part. Although CE marking is not specified, the Class I classification requires compliance with current hygiene standards. It is recommended to follow the sterilization instructions from the manufacturer Hu-Friedy to preserve the integrity of the instrument and guarantee patient safety. Regular inspection of the working tip is advised to maintain optimal efficiency during cement removal.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed under Class I, which corresponds to products presenting a low degree of risk according to medical device regulations. Hu-Friedy is a globally recognized brand for the quality of its manual instrumentation. The product is intended exclusively for professional use by trained practitioners. Any use must be preceded by a careful reading of the instructions for use provided by Hu-Friedy to guarantee an application compliant with the safety and clinical efficacy standards expected in dental surgery.
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Specifications
| Manufacturer | Hu-Friedy |
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