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Diamond Removable Points 2.35 mm - Helmut Zepf (31.185.10) - Delynov

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The Pointes diamantées amovibles 2,35 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 31.185.10.
  • Reserved for healthcare professionals. Read instructions carefully before use.

159.01 € 159.01 EUR 159.01 € Tax Included

159.01 € Tax Included

(159.01 € / Units)
  • Manufacturer

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Instrument

What are Helmut Zepf removable diamond tips?

The 2.35 mm removable diamond tips, referenced under code 31.185.10, are rotary instruments designed by Helmut Zepf Medizintechnik GmbH. Manufactured from high-quality medical stainless steel, these tips are intended to be mounted on compatible manual instruments for precision interventions. They belong to the consumables category (CONSO) and are classified as Class I medical devices. This equipment is delivered non-sterile and requires a complete preparation protocol before any clinical use. The removable structure allows for flexible management of instrumentation according to the specific needs of the practitioner during care.

What are the clinical indications?

The intended use for these dental diamond tips is as a manual rotary dental instrument. They are indicated for oral surgery, implantology, or periodontology procedures requiring an abrasion or rectification action. The manufacturer Helmut Zepf specifies that the use of these devices is strictly reserved for qualified healthcare professionals. They are used in surgical site preparation protocols or for the adjustment of prosthetic and anatomical structures. It is imperative to verify compatibility with other products and instruments used during the procedure to ensure optimal operative safety.

What are the technical characteristics?

These diamond tips (reference 31.185.10) feature a standard shank diameter of 2.35 mm, ensuring compatibility with conventional dental rotary systems. They are composed of medical stainless steel, a material chosen for its resistance to thermal and chemical treatment cycles. The manufacturer Helmut Zepf Medizintechnik GmbH emphasizes that, although there is no defined maximum limit for treatment cycles due to the design and materials, the user must inspect each product before use. Any sign of visible damage, such as cracks, breaks, or defects on the cutting edges, must lead to the immediate withdrawal of the instrument.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer concerns hypersensitivity reactions. Contact with the instrument may cause metal intolerance in certain patients, as the instrument is manufactured from medical stainless steel. If such an allergic or hypersensitivity reaction is triggered during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, it is strictly forbidden to use damaged or worn products. A systematic check of the integrity of the diamond tip is therefore required before each surgical act to avoid any risk of complication.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile. According to the manufacturer's safety instructions, all instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as before each subsequent use. The cleaning process must be complete and rigorous to eliminate all residues. It is crucial to inspect the instrument to detect any potential wear or alterations of the diamond surfaces. Due to the nature of the materials used, the number of achievable reprocessing cycles depends on the physical condition of the instrument, and no fixed limit is defined by the manufacturer, leaving the assessment of wear to the responsibility of the healthcare professional.

Who is the manufacturer and what standards are respected?

These instruments are manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer respects manufacturing standards for Class I medical devices. The products are designed to meet the safety and performance requirements of dental surgery professionals. Although the specific CE marking is not detailed in the provided source data, compliance with directives relating to manual instruments in medical stainless steel is ensured by Helmut Zepf's rigorous manufacturing protocols. Each device is identified by a precise technical reference (31.185.10) allowing for adequate traceability within the dental practice.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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