Goldman-Fox/Williams Probe #GF/W #6 Handle 1-2-3-5-7-8-9-10 - Hu-Friedy - Delynov
The Sonde Goldman-Fox/Williams #GF/W manche #6 10-9-8-7-5-3-2-1 - 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 Goldman-Fox/Williams #GF/W probe with handle #6?
The Goldman-Fox/Williams #GF/W probe from the brand Hu-Friedy is a manual diagnostic instrument designed for periodontology and implantology. This device is characterized by a double end combining two types of recognized graduations. It has a #6 diameter handle, offering a specific grip for clinical examinations. Manufactured by Hu-Friedy Mfg. Co., LLC, this Williams and Goldman-Fox periodontal probe is an essential measurement tool for evaluating biological space and the health of supporting tissues. Its rigid structure allows for precise tactile exploration of root surfaces and bone crevices during initial assessments or post-operative re-evaluations.
What are the clinical indications for this instrument?
The use of the Goldman-Fox and Williams probe is indicated for the millimeter measurement of periodontal pocket depth and gingival recession. In oral surgery and implantology, it allows for checking the height of keratinized gingiva and planning implant positioning based on available biological space. It is also used for screening attachment loss and monitoring healing after root planing or flap surgery. This instrument is reserved exclusively for qualified healthcare professionals, in accordance with Hu-Friedy manufacturer guidelines, to ensure reliable diagnosis and safe handling of soft tissues.
What are the technical characteristics of the graduations?
This Williams periodontal probe features specific technical marking characteristics with a 10-9-8-7-5-3-2-1 graduation sequence. These visual cues allow the practitioner to precisely quantify clinical dimensions in millimeters. The combination with the Goldman-Fox profile offers increased versatility when examining different quadrants or varied gingival morphologies. The Hu-Friedy handle number 6 is designed to facilitate control during insertion into the sulcus, allowing for a clear reading of measurements without exerting excessive pressure on the connective attachment. Marking precision is a critical element for the reproducibility of measurements during longitudinal follow-up of patients with periodontitis.
What are the contraindications for the use of this probe?
According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not listed beyond use restricted to healthcare professionals. However, from a clinical perspective, the use of the Williams periodontal probe may be limited in areas of acute purulent periodontitis or undrained periodontal abscess to avoid causing unnecessary pain or deep bacterial dissemination without prior control. It is imperative to read the instructions carefully before use to comply with sterilization and instrument maintenance protocols, thereby ensuring the absence of cross-contamination and the integrity of the examined tissues.
What are the maintenance precautions for this non-absorbable instrument?
As this is a manual metal instrument and not a suture, precautions mainly concern decontamination and sterilization. The Hu-Friedy Goldman-Fox probe must be cleaned and sterilized between each patient according to standard dental office hygiene protocols. The integrity of the millimeter graduations should be checked regularly, as wear or discoloration of the markings could distort clinical measurements. Particular attention must be paid to the working end to ensure it is neither bent nor blunt, which would alter probing precision and could traumatize gingival tissues during insertion into the periodontal pocket.
Who is the manufacturer and what standards are met?
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 belongs to Class I according to current regulations. As a Class I product, it meets the safety and performance requirements defined for reusable manual surgical instruments. Although CE marking is not explicitly specified in the source data, compliance with Hu-Friedy manufacturer standards ensures rigorous manufacturing quality. Professionals must refer to the instructions for use and manufacturer warnings to ensure use compliant with international dental and periodontal practice standards.
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Specifications
| Manufacturer | Hu-Friedy |
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