Periodontal Probe Contrast - Helmut Zepf (24.451.06) - Delynov

What is the Helmut Zepf contrast periodontal probe?

The Helmut Zepf contrast periodontal probe, referenced under code 24.451.06, is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this probe is specifically developed for the clinical examination of the tooth's supporting tissues. It belongs to the consumables category (CONSO) and is classified as a Class I medical device. Its structure is optimized to offer increased visibility during intraoral measurements, thus facilitating the practitioner's work during diagnostic or periodontal follow-up phases.

What are the clinical indications for this instrument?

The intended use for this manual instrument is strictly limited to dental interventions. In clinical practice, the contrast periodontal probe is used to measure the depth of the sulcus or periodontal pockets, evaluate the level of gingival recession, and detect potential loss of attachment. It is essential during initial examinations to establish a complete periodontal diagnosis, as well as during post-operative follow-up visits or implant maintenance. Its use is reserved exclusively for health professionals qualified in oral and dental surgery.

What are the technical characteristics of the 24.451.06 probe?

The Helmut Zepf contrast periodontal probe is distinguished by its medical grade stainless steel construction, ensuring resistance to repeated reprocessing cycles. As a manual instrument, it offers a precise tactile response during the exploration of periodontal pockets. The manufacturer Helmut Zepf delivers this product non-sterile, which requires a strict preparation protocol before the first use. The design of the instrument does not define a maximum limit for treatment cycles, as this depends on visible wear and the care taken during cleaning and sterilization.

What are the contraindications for using this probe?

The main medical contraindication mentioned by the manufacturer concerns hypersensitivity or metal intolerance. Since the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the examination, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore recommended to question the patient about their history of metal allergies before any clinical handling with this instrument.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is crucial to visually inspect the product before each intervention to detect any potential damage or visible wear, such as cracks, breaks, or defects on the active parts. Never use damaged or worn products. The reprocessing process must be complete and rigorous to ensure patient safety and the longevity of the stainless steel instrument, in accordance with the manufacturer's safety instructions.

Who is the manufacturer and what standards are respected?

This medical device is manufactured by Helmut Zepf Medizintechnik Gmbh, located in Seitingen-Oberflacht, Germany. The product complies with medical device regulations and is registered as Class I. As a manual dental instrument, it meets the quality requirements of the medical stainless steel used by the brand. Health professionals must refer to the instructions provided by Helmut Zepf to ensure use in accordance with the intended purpose. Traceability is ensured by technical reference 24.451.06, guaranteeing the origin and conformity of the equipment provided by Delynov.

State of the art

Surgical medical consumables play a decisive role in operative safety.