Williams periodontal probe #6 handle 1-2-3-5-7-8-9-10 Qulix
The Sonde paro Williams manche #6 1-2-3-5-7-8-9-10 Qulix 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.
| Manufacturer: Hu-Friedy |
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What is the Williams probe handle #6 1-2-3-5-7-8-9-10 Qulix?
The Williams probe from the Hu-Friedy brand is a periodontal diagnostic instrument designed to accurately measure pocket depth and epithelial attachment. This specific model is distinguished by its Qulix marking, a color-coded graduation technology offering increased visibility during clinical examination. It is equipped with a #6 type handle, providing a volume adapted to the practitioner's hand for controlled manipulation. Manufactured under the aegis of the manufacturer Hu-friedy, this instrument is a Class I medical device intended exclusively for professional use in dental offices or hospital settings for periodontology and implantology procedures.
What are the clinical indications?
The use of this Williams probe is indicated for the systematic evaluation of patients' periodontal health. It allows for quantifying attachment loss, detecting bleeding on probing, and measuring gingival recession. In oral and implant surgery, it is used to verify the depth of peri-implant tissues and to plan tissue regeneration interventions. The Hu-Friedy brand offers this tool to assist in the early screening of periodontal diseases and post-operative follow-up. Its use is reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer located in Chicago, USA, to ensure reliable clinical interpretation of the measurements obtained.
What are the technical characteristics?
This periodontal probe features specific graduations according to the Williams sequence: 1, 2, 3, 5, 7, 8, 9, and 10 mm. The absence of the 4 and 6 mm marks is a specific characteristic of this type of probe to facilitate quick reading of certain critical depths. The Qulix system uses durable pigments to ensure the longevity of the marking despite repeated sterilization cycles. The number 6 handle is designed to offer optimal balance during passage through the different quadrants of the oral cavity. As a product of the Hu-Friedy brand, this instrument respects the rigorous manufacturing standards imposed for Class I devices, ensuring compliance with current regulatory requirements.
What are the contraindications for use?
According to information provided by the manufacturer Hu-friedy, the use of this instrument is strictly reserved for trained healthcare professionals. Although the raw MDR text does not list specific medical contraindications related to the patient's condition (such as allergies to materials not specified here), it is imperative not to use the instrument in case of visible damage to the tip or graduations, which could distort measurements or traumatize soft tissues. The practitioner must systematically refer to the instructions for use before any intervention to ensure the device's suitability for the encountered clinical situation and respect standard asepsis protocols.
What are the maintenance and durability precautions?
As a non-resorbable and reusable instrument, this Class I Williams probe requires rigorous decontamination and sterilization between each patient. It is essential to follow the manufacturer Hu-friedy's instructions for cleaning to preserve the integrity of the Qulix marking and the #6 handle. Regular visual inspection is recommended to check for the absence of corrosion or dulling of the probing tip. The accuracy of measurements depends directly on maintaining the straightness of the working part. Any structural deformation must lead to the immediate disposal of the instrument to guarantee patient safety and the reliability of the periodontal diagnosis.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device, meeting the regulatory safety and performance requirements for manual surgical instruments. The Hu-Friedy brand ensures the distribution of this diagnostic tool to dental surgeons and periodontists. Professionals must imperatively read the instructions carefully before use to comply with warnings and intended usage protocols. Traceability and compliance with American and international manufacturing standards are guaranteed by the quality control processes of the manufacturer Hu-friedy.
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