Kramer #1 curette #6 handle

What is the Kramer #1 curette #6 handle?

The Kramer #1 curette #6 handle, distributed under the Hu-Friedy brand, is a precision manual instrument intended for the oral surgery sector. This device consists of a working part specific to the Kramer #1 model, mounted on a #6 type handle, recognized for its grip adapted to prolonged clinical acts. This Hu-Friedy brand instrument is designed for procedures requiring rigorous manipulation of periodontal tissues. As a medical device, it meets the manufacturing standards of the manufacturer located in the United States. Its structure allows access to complex anatomical areas to perform deep cleaning of roots or sockets during surgical procedures.

What are the clinical indications?

The clinical indications for the Kramer #1 curette #6 handle from the Hu-Friedy brand primarily concern periodontology and oral surgery. It is indicated for the removal of subgingival calculus, root planing, and curettage of granulation tissue in periodontal pockets or extraction sites. Its use is particularly relevant during biological preparation phases before implant placement or during flap surgeries. This Hu-Friedy device is exclusively reserved for qualified healthcare professionals, such as dental surgeons and implantologists, who master manual debridement techniques to ensure the cleaning of the tooth's supporting tissues.

What are the technical characteristics?

The Kramer #1 curette #6 handle features technical specifications defined by the manufacturer Hu-friedy. It is an instrument classified as Class I according to medical device regulations. The Kramer #1 working part is associated with a number 6 handle, a standard configuration that prioritizes tactile control during the application of curettage forces. Although the exact composition is not specified in the source data, this instrument is designed to withstand the sterilization cycles required in a dental office. Each unit is manufactured under the rigorous control of the manufacturer in Chicago, guaranteeing compliance with the requirements of the INSTRU category for invasive devices for temporary surgical use.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not listed exhaustively beyond general warnings. However, the use of the Kramer #1 curette #6 handle is strictly reserved for healthcare professionals. An implicit contraindication lies in the use by unqualified personnel or for an application not in accordance with the intended purpose of the instrument. It is imperative to read the instructions carefully before use to identify any restrictions related to the patient's clinical state or specific surgical protocols. As with any sharp manual instrument, inappropriate use could damage dental or periodontal structures.

What are the precautions for use and maintenance?

As the Kramer #1 curette #6 handle is a non-absorbable instrument of the INSTRU category, it requires a strict maintenance protocol between each patient. Although reprocessing details are not detailed in the raw text, professional use implies systematic decontamination, cleaning, and sterilization in accordance with Hu-friedy manufacturer guidelines. Practitioners must inspect the integrity of the Kramer #1 working part before each intervention to ensure its sharpness and the absence of corrosion. Being a Class I device, its maintenance must comply with current hygiene standards in dental surgery to prevent the risks of cross-infection and guarantee patient safety.

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 medical device is listed under Class I, which confirms its compliance with basic regulatory requirements for manual surgical instruments. The Kramer #1 curette #6 handle is distributed under the Hu-Friedy brand and is part of a strict regulatory framework intended for healthcare professionals. Although specific CE marking is not mentioned in the source data, the product follows the indications and warnings provided by the manufacturer to ensure safe and effective use in a clinical setting. Traceability is ensured by the technical references of the American manufacturer.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.