Probe number 8 handle number 6 - Hu-Friedy - Delynov
The Sonde #8 manche #6 - 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.
| Manufacturer: Hu-Friedy |
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What is the Hu-Friedy probe #8 handle #6?
The probe #8 handle #6 is a manual diagnostic instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device consists of a specific working part, the dental probe n8, mounted on a #6 type handle. The manufacturer Hu-Friedy uses rigorous manufacturing processes to guarantee the reliability of this instrument intended for clinical exploration. As a Class I device, it meets the basic regulatory requirements for non-invasive or temporarily invasive instruments used in dental practices. Its structure is designed to offer a grip adapted to routine diagnostic acts in oral surgery and periodontology.
What are the clinical indications?
This dental probe n8 is primarily indicated for the exploration of dental surfaces, the detection of caries, as well as the examination of restoration margins. In periodontology and implant surgery, it is used to evaluate the texture of hard tissues and identify the presence of subgingival calculus or other anatomical anomalies. Practitioners use this Hu-Friedy instrument during initial diagnostic phases or post-operative follow-up to check the condition of treated structures. Its use is strictly reserved for qualified healthcare professionals, in accordance with the manufacturer's recommendations for interventions in the oral environment.
What are the technical characteristics?
The probe #8 handle #6 is distinguished by the configuration of its active tip, referenced under number 8, which allows for fine tactile exploration. The number 6 handle is designed to ensure stable handling during the clinical examination. This medical device belongs to Class I according to the current regulatory classification. Manufactured by Hu-Friedy Mfg. Co., LLC in the United States, this instrument benefits from the technical expertise of a recognized manufacturer in the field of surgical instrumentation. Although specific material details are not listed in the source data, the design complies with Hu-Friedy industrial standards for manual diagnostic instruments.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond general warnings. However, the use of this instrument is prohibited for any use other than that intended, namely dental diagnosis and exploration by a trained professional. The device should not be used if the integrity of the tip or handle is compromised, in order to avoid any risk to the patient. Practitioners must systematically refer to the instructions for use provided by Hu-Friedy Mfg. Co., LLC to ensure the suitability of the instrument for the clinical situation encountered and the patient's health status.
What are the maintenance and handling precautions?
As a non-resorbable and reusable instrument, the dental probe n8 requires a strict sterilization and cleaning protocol between each patient. Although specific resorption precautions do not apply here, maintaining the precision of the #8 tip is essential to guarantee diagnostic reliability. Hu-Friedy recommends reading the instructions carefully before use to become familiar with the appropriate decontamination cycles. Careful handling preserves the physical properties of the #6 handle and the tactile acuity of the probe. Any sign of wear or corrosion must lead to the immediate replacement of the instrument to maintain the safety of care.
Who is the manufacturer and what standards are respected?
The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, IL 60618, USA. This product is classified as a Class I medical device. Compliance with standards is ensured by the quality control processes of Hu-Friedy, a globally recognized manufacturer in the dental sector. Although specific CE marking is not mentioned in the current technical sheet, the device complies with regulatory requirements for instruments of its class for safe marketing. Healthcare professionals must consult the technical documentation and instructions for use provided by the manufacturer to ensure use in accordance with current safety standards.
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