Simple graduated probe CPG 12 3-6-9-12 Helmut Zepf (24.453.12) - Delynov Delynov

What is the Helmut Zepf CPG 12 single graduated probe?

The CPG 12 single graduated probe is a manual diagnostic instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device, referenced under code 24.453.12, is manufactured from high-quality medical stainless steel to ensure resistance to repeated sterilization processes. Its fine structure and blunt tip allow for atraumatic exploration of soft tissues. It is distinguished by its specific graduated markings at 3, 6, 9, and 12 mm, facilitating a quick and precise reading of clinical measurements during periodontal examinations.

What are the clinical indications?

In oral surgery and periodontology, the cpg 12 probe is indicated for evaluating the health of the tooth's supporting tissues. It is primarily used to measure the depth of the sulcus or periodontal pockets, assess the level of epithelial attachment, and detect the presence of bleeding on probing. This instrument is essential during the diagnostic, implant or periodontal treatment planning phases, as well as for post-operative follow-up and long-term maintenance of patients with periodontitis.

What are the technical characteristics?

The cpg 12 periodontal probe (reference 24.453.12) features technical characteristics optimized for clinical precision. It has a simplified CPG-type graduation with increments at 3-6-9-12 mm, allowing for immediate identification of critical pocket depth thresholds. Manufactured by Helmut Zepf, it is designed in medical stainless steel, offering excellent durability and corrosion resistance. This device is classified as a Class I instrument according to current regulations, ensuring its compliance with safety requirements for non-invasive manual instruments.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity to metals. An intolerance reaction may occur in some patients upon contact with the medical stainless steel constituting the instrument. If such a hypersensitivity reaction is triggered during the examination, the procedure must be immediately stopped and the necessary clinical measures must be taken. It is therefore recommended to question the patient about their allergic history before any manipulation of the instrument in the mouth.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use as well as between each patient. Before any treatment cycle, the instrument must be visually inspected to detect potential damage such as cracks, breaks, or defects on the active areas. The use of damaged or worn products is strictly prohibited. Due to its stainless steel design, there is no defined maximum limit for reprocessing cycles, as long as the physical integrity of the probe is preserved.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to certain reprocessing nomenclatures). As a manual instrument intended for healthcare professionals, it meets the rigorous manufacturing requirements for medical stainless steel. The manufacturer emphasizes that the use of this instrument is strictly reserved for qualified healthcare professionals, thus ensuring an application compliant with periodontal and dental surgery clinical protocols.

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