Langer curette #3/4 handle #7
The Curette Langer #3/4 manche #7 is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Langer #3/4 curette handle #7?
The Langer #3/4 curette handle #7, marketed by the brand Hu-Friedy, is a manual instrument used in periodontology and oral surgery. Its structure combines the design characteristics of a universal curette with the specific angles of Gracey curettes, thus offering increased versatility for the treatment of periodontal pockets. This particular model is mounted on a number 7 handle, providing a grip adapted to the requirements of meticulous clinical interventions. As a medical device developed by a recognized manufacturer, this instrument is designed to meet the needs of practitioners demanding high-quality periodontal instrumentation.
What are the clinical indications?
The use of the Langer #3/4 curette from the brand Hu-Friedy is indicated for periodontal debridement and root planing, primarily in the posterior sectors of the oral cavity. It is particularly effective for the removal of calcified deposits and subgingival calculus on the root surfaces of molars and premolars. In implant and periodontal surgery, it is used in site preparation and the cleaning of infected tissues. Its use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-friedy located in Chicago, USA, ensuring application consistent with current clinical standards.
What are the technical characteristics?
The Langer #3/4 curette is distinguished by its double working end, allowing for the treatment of opposite faces without changing instruments. Unlike Gracey curettes which are face-specific, the Langer has a universal blade with two cutting edges and a flat face at 90 degrees relative to the lower shank. This technical configuration allows for optimal angulation when moving from mesial to distal areas of the posterior teeth. The #7 handle associated with this Hu-Friedy model ensures precise handling during curettage procedures. The instrument is classified as a Class I device according to current regulations.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, specific contraindications are not detailed beyond the general framework of the intended use. However, the use of this instrument from the brand Hu-Friedy must be avoided by any person who does not have the qualification of a healthcare professional. It is imperative to refer to the instructions for use before any intervention. Usual contraindications in manual instrumentation include use on non-target structures or in clinical situations where tissue integrity does not allow for the application of controlled mechanical force. A prior clinical evaluation is necessary to validate the relevance of the instrumentation.
What are the maintenance and durability precautions?
Although this Class I device is non-resorbable, its durability and effectiveness directly depend on the sterilization and maintenance protocols followed by the practice. As a precision metallic instrument, the Langer #3/4 curette requires rigorous cleaning after each use to remove organic debris before the sterilization cycle. It is recommended to scrupulously follow the cleaning and disinfection instructions provided by the manufacturer Hu-friedy to preserve the sharpness of the blades and the integrity of the #7 handle. Regular inspection of the cutting edges is advised to ensure effective and safe root planing for the patient.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-friedy, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product belongs to the INSTRU category and is regulated as a Class I medical device. Compliance with manufacturing standards ensures that the Langer #3/4 curette meets the safety and performance requirements for use in a clinical setting. It is reminded that this device is exclusively reserved for healthcare professionals. Although CE marking is not specified in the source data, compliance with Class I indicates adherence to the rigorous quality control processes imposed for manual surgical instruments.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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