Single graduated probe CP 12 3-6-9-12 - Helmut Zepf (24.453.22) - Delynov
The Sonode graduée simple CP 12 3-6-9-12 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.453.22.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf CP 12 single graduated probe?
The CP 12 single graduated probe, referenced under code 24.453.22, is a manual instrument designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, it features a fine and rigid structure adapted for the exploration of periodontal tissues. This device is distinguished by its specific graduations located at 3mm, 6mm, 9mm, and 12mm, allowing for rapid and standardized reading during clinical examinations. As a diagnostic instrument, it is essential for evaluating the health status of the tooth's supporting tissues. Its monobloc design ensures optimal tactile transmission for the practitioner during insertion into the sulcus or periodontal pocket.
What are the clinical indications for this instrument?
This probe is indicated for complete periodontal examination in oral surgery and general practice. Its primary use lies in measuring the probing depth of periodontal pockets, a crucial step for the diagnosis of periodontitis. It also allows for measuring gingival recessions, evaluating furcation involvement, and checking the stability of peri-implant tissues. The Helmut Zepf instrument helps the clinician establish a precise periodontal assessment (charting) and monitor the effectiveness of non-surgical or surgical treatments over follow-up sessions. Its use is reserved exclusively for qualified healthcare professionals.
What are the technical characteristics of the 24.453.22 probe?
The Helmut Zepf 24.453.22 probe is a non-sterile Class I instrument. It is designed from high-quality medical stainless steel to withstand repeated reprocessing cycles. The working part is equipped with CP 12 graduations (3-6-9-12 mm) which offer clear visual aid for quantifying attachment loss. Its fineness allows for atraumatic penetration into the biological space while maintaining the necessary rigidity for reliable measurement. The manufacturer specifies that the instrument must be inspected before each use to detect any visible damage such as cracks, breaks, or defects on the edges, in order to guarantee patient safety.
What are the contraindications for the use of this probe?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals, particularly the medical stainless steel used for the manufacture of the instrument. If a hypersensitivity reaction is triggered in the patient upon contact, the clinical procedure must be immediately stopped. Necessary medical measures must then be taken accordingly. It is therefore recommended to question the patient about their history of metal allergies before any intervention with this manual instrument.
What are the maintenance and sterilization precautions?
Like all instruments of the Helmut Zepf brand, this probe is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as after each subsequent use. Reprocessing must follow standard hospital protocols for reusable medical devices. Due to its design and the materials used, there is no defined maximum limit for the number of treatment cycles, but the instrument must be discarded in case of visible wear or degradation of the graduations. Compatibility with other cleaning products must also be verified beforehand.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product belongs to Class I according to the current regulations on medical devices. The manufacturer follows rigorous quality control protocols to ensure the compliance of its manual instruments. As a Class I device, it meets the safety and performance requirements for manual dental instruments. Professionals must refer to the manufacturer's instructions for cleaning and sterilization (MDC0483) in order to maintain the integrity of the medical stainless steel over time.
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Specifications
| Manufacturer | Helmut Zepf |
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