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Contrast Periodontal Probe - Helmut Zepf (24.451.01) - Delynov

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The Sonde parodontale contraste - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.451.01.
  • Reserved for healthcare professionals. Read instructions carefully before use.

117.05 € 117.05 EUR 117.05 € Tax Included 229.52 €

117.05 € Tax Included 229.52 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf contrast periodontal probe?

The Helmut Zepf contrast periodontal probe, referenced under code 24.451.01, is a manual periodontal diagnostic instrument. Designed by Helmut Zepf Medizintechnik GmbH, it is manufactured from high-quality medical stainless steel, ensuring resistance adapted to clinical practice requirements. This device belongs to the consumables category and is classified as a Class I medical device. Its specific design with contrast allows the practitioner to perform precise measurements and observations during examinations of the oral cavity. As a non-sterile instrument upon delivery, it requires a complete reprocessing protocol before its first use and between each patient.

What are the clinical indications for this instrument?

This instrument is primarily indicated for interventions related to periodontal treatments. Its intended purpose includes probing gingival pockets to assess attachment loss depth and the health status of the periodontium. Beyond its diagnostic function, the Helmut Zepf probe is also used for the mechanical removal of tartar, whether soft or hard, on natural teeth or dental appliances. It thus allows the dental surgeon to intervene directly on the dental apparatus to clean areas infected or cluttered by calcified deposits, facilitating the overall management of periodontal pathologies in the office.

What are the technical characteristics of the 24.451.01 probe?

The Helmut Zepf periodontal probe is characterized by its composition in medical stainless steel, a standard material for surgical instrumentation ensuring durability against sterilization cycles. Although the manufacturer does not define a strict maximum limit for the number of processing cycles, the instrument's lifespan depends on the absence of visible damage such as cracks, breaks, or defects on the edges. It is a Class I instrument, delivered non-sterile. Its ergonomic design is intended for precision work on soft tissues and hard surfaces, providing the necessary tactile response when probing gingival pockets.

What are the contraindications for the use of this probe?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity to materials. Contact with medical stainless steel can cause metal intolerance reactions in certain sensitive patients. If a hypersensitivity reaction is triggered during examination or treatment, the procedure must be stopped immediately. The practitioner must then take the necessary measures to manage the allergic reaction. 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 reprocessing precautions?

Like any reusable Helmut Zepf instrument, this probe must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The reprocessing process must be complete to ensure the safety of the patient and the practitioner. Before each use, a visual inspection is mandatory to detect any wear, cracks, or alteration of the cutting edges. The use of damaged or worn products is strictly prohibited. Due to the quality of the materials used, the number of achievable treatment cycles cannot be fixed, but remains conditioned by the physical state of the instrument observed by the healthcare professional.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This product complies with the regulations for Class I medical devices. The manufacturer emphasizes that the use of this instrument is strictly reserved for qualified healthcare professionals. Compliance with cleaning and sterilization protocols is the responsibility of the practitioner, in accordance with the instructions provided by Helmut Zepf. Traceability is ensured by the technical reference 24.451.01, allowing for the precise identification of the model within the brand's range of periodontal instruments.


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Manufacturer Helmut Zepf
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