Probe number 6L, handle number 30, 9mm - Hu-Friedy - Delynov

What is the #6L probe #30 handle 9mm - Hu-Friedy?

The #6L probe #30 handle 9mm developed by Hu-Friedy is a manual diagnostic instrument used in periodontology. This device consists of a working part calibrated at 9mm and a #30 type handle. Designed by Hu-Friedy Mfg. Co., LLC, this 9mm dental probe is structured to offer an accurate reading of clinical measurements within the oral cavity. As an instrument in the INSTRU category, it meets the manufacturing requirements of a recognized player in the dental sector, guaranteeing standardized integration into the dentist's technical tray for routine examinations or post-operative follow-ups.

What are the clinical indications for this 9mm periodontal probe?

The use of this millimeter dental probe is primarily indicated for assessing the health status of the tooth's supporting tissues. In oral surgery and periodontology, it allows for measuring the depth of the sulcus or periodontal pockets up to 9mm. It is also used to identify clinical attachment loss, evaluate gingival recessions, and check for bleeding on probing. Its precision is fundamental for establishing a complete periodontal diagnosis, planning debridement treatments, or ensuring the monitoring of peri-implant tissue stability during maintenance phases.

What are the technical characteristics of this Hu-Friedy instrument?

The #6L probe is distinguished by its specific 9mm calibration, allowing for precise millimeter evaluation. It is mounted on a #30 handle, a technical reference at Hu-Friedy designed for daily clinical handling. This device is part of Class I according to the regulatory classification of medical devices. The design of the working part is optimized to access different areas of the dental arch while transmitting the tactile information necessary for the practitioner to detect subgingival deposits or root structure anomalies. The manufacturing quality of Hu-Friedy Mfg. Co., LLC ensures compliance with the standards expected for manual diagnostic instruments.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed for the use of this probe, outside of standard clinical practice protocols. However, the use of this instrument is strictly reserved for qualified healthcare professionals. It is imperative to read the instructions carefully before use to comply with safety guidelines. As with any invasive diagnostic instrument, use must be adapted to the state of the patient's soft tissues to avoid any unnecessary trauma during probing, particularly in the presence of acute inflammation or fragile tissues.

What are the precautions for use and maintenance for this probe?

Although this product is classified as non-resorbable (being a manual instrument and not a suture), rigorous precautions must be observed. As a Class I device, the probe must be cleaned, disinfected, and sterilized before each use in accordance with the protocols in force in the dental office and the instructions from the manufacturer Hu-Friedy. The practitioner must check the integrity of the 9mm millimeter graduation before each examination to guarantee the reliability of the measurements. Careful handling is required to preserve the fineness of the tip and avoid any deformation that could distort the periodontal diagnosis or damage the epithelial attachment.

Who is the manufacturer and what standards are respected by this product?

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 under Class I. The Hu-Friedy brand is recognized worldwide for the manufacture of high-quality surgical and diagnostic instruments. Compliance with Class I manufacturing standards ensures that the product meets the safety and performance requirements defined for non-invasive or diagnostic instruments used by healthcare professionals. Practitioners should refer to the technical documentation and the instructions for use provided by the manufacturer to ensure use in compliance with health regulations.

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