Periodontal Probe #23 handle #7 12-9-6-3

What is the Periodontal Probe #23 handle #7 12-9-6-3?

The Periodontal Probe #23 handle #7 12-9-6-3 is a manual diagnostic instrument developed by the brand Hu-Friedy. This medical device belongs to the INSTRU category and is distinguished by its specific configuration combining an exploring tip and a millimeter graduation. Its structure is designed to offer a precise tactile response during the examination of soft tissues and dental surfaces. Used daily in oral surgery, this probe from the brand Hu-Friedy meets the handling requirements of practitioners for the evaluation of periodontal health. As a Class I device, it is subject to rigorous manufacturing protocols guaranteeing its reliability during routine clinical procedures or during complete assessments before an implant intervention.

What are the clinical indications?

The clinical indications for this instrument from the brand Hu-Friedy primarily concern periodontal diagnosis and monitoring. The Periodontal Probe #23 handle #7 12-9-6-3 is indicated for measuring periodontal pocket depth, evaluating the epithelial attachment level, and detecting horizontal or vertical bone loss. It is also used to identify the presence of subgingival calculus or potential furcation involvement. In implant surgery, it allows for checking the thickness of soft tissues and the stability of the gingival level around the abutments. Its use is strictly reserved for qualified healthcare professionals, in accordance with the manufacturer's directives, to ensure accurate clinical data collection essential for establishing an appropriate periodontal or surgical treatment plan.

What are the technical characteristics?

The Periodontal Probe #23 handle #7 12-9-6-3 features technical specifications adapted to the oral anatomy. It has a sequential graduation of the 12-9-6-3 type, allowing for rapid and standardized reading of probing depths during clinical examination. The #7 handle offers a grip that facilitates control of the movement and the transmission of tactile sensations when passing into the gingival-dental sulcus. This instrument is classified as a Class I device according to current regulations. The design of the working part allows access to different areas of the dental arch with great maneuverability. The manufacturing quality ensured by the manufacturer guarantees that the instrument retains its physical properties and readability after the cleaning and sterilization cycles required in the dental office.

What are the contraindications for use?

According to the information provided by the manufacturer, specific contraindications are not detailed beyond the general framework of use for manual diagnostic instruments. However, the use of the Periodontal Probe #23 handle #7 12-9-6-3 should be avoided on tissues presenting uncontrolled acute inflammation if probing risks causing excessive trauma, unless immediate diagnosis is necessary. It is the practitioner's responsibility to judge the relevance of the examination based on the patient's clinical state. The manufacturer specifies that this device is exclusively reserved for healthcare professionals. Inappropriate use or use by unqualified personnel constitutes a major contraindication, as it could lead to diagnostic errors or iatrogenic lesions to the periodontal ligament or the gingival attachment.

What are the maintenance and handling precautions?

As a non-absorbable and reusable instrument, the Periodontal Probe #23 handle #7 12-9-6-3 requires a strict maintenance protocol between each patient. Although it is not a suture, handling precautions are essential to preserve the integrity of the 12-9-6-3 graduation and the fineness of the tip. It is imperative to read the instructions carefully before use to comply with the decontamination, cleaning, and sterilization cycles recommended by the manufacturer located in Chicago, USA. Any sign of wear, corrosion, or deformation of the working part must lead to the withdrawal of the instrument to guarantee the precision of measurements. Compliance with these procedures ensures the longevity of the device and microbiological safety within the dental surgery office.

Who is the manufacturer and what standards are respected?

The Periodontal Probe #23 handle #7 12-9-6-3 is produced by the manufacturer Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed under Class I, which implies compliance with basic regulatory requirements for non-invasive or short-term invasive surgical instruments. The manufacturer is internationally recognized for its production standards in the field of dental instrumentation. Compliance with standards is attested by adherence to the indications and warnings provided in the technical documentation. Healthcare professionals must systematically refer to the instructions for use to guarantee use in accordance with the safety and performance expectations defined by the manufacturer for this category of diagnostic instruments.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.