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Clamps Ivory Holder - Helmut Zepf (19.037.01) - Delynov

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The Pinces porte-IVORY - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.037.01.
  • Reserved for healthcare professionals. Read instructions carefully before use.

92.72 € 92.72 EUR 92.72 € Tax Included

92.72 € Tax Included

(92.72 € / Units)
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Instrument

What is the Helmut Zepf IVORY clamp forceps (19.037.01)?

The IVORY clamp forceps, referenced under code 19.037.01 by Helmut Zepf, is a manual dental instrument specifically designed for handling operative field accessories. Manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this ivory clamp forceps features a robust structure adapted to the constraints of daily clinical practice. It allows the practitioner to grasp, spread, and position clamps in a controlled manner. As a Class I device, it meets the safety and performance requirements for non-invasive or invasive instruments for temporary use in the oral cavity.

What are the clinical indications for this instrument?

This instrument is primarily indicated for the placement and removal of clamps during the installation of a dental dam. Its use is essential in procedures requiring perfect isolation of the operative field, such as endodontic treatments, adhesive restorations, or certain stages of conservative surgery. The ivory clamp forceps allows for maintaining adequate tension on the clamp to cross interdental contact points without damaging the surrounding soft tissues. Its role is crucial to ensure the seal and stability of the isolation device throughout the duration of the procedure.

What are the technical characteristics of the ivory clamp forceps?

The Helmut Zepf ivory clamp forceps is distinguished by its ergonomic medical stainless steel design, guaranteeing optimal resistance to corrosion and repeated sterilization cycles. Its geometry is designed to adapt to the majority of standard clamps on the market. The locking or spring mechanism allows the clamp to be held open without excessive effort from the practitioner, thus offering increased visibility during cervical adjustment. The surface finish is treated to limit reflections under operative lighting, while facilitating the cleaning and decontamination steps provided by the manufacturer.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns the patient's known hypersensitivity to metals. Since the instrument is composed of medical stainless steel, an allergic reaction may occur upon contact with mucous membranes or dental tissues. If a hypersensitivity reaction is triggered during use, the procedure must be immediately stopped and necessary clinical measures must be taken. It is also contraindicated to use the instrument if it shows visible damage, such as cracks, breaks, or defects on the active parts, as this could compromise patient safety and the effectiveness of the procedure.

What are the maintenance and reprocessing precautions?

Like any reusable manual dental instrument, the ivory clamp forceps must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer specifies that it is crucial to perform a complete cleaning to remove all organic residue before the sterilization cycle. Due to the quality of the materials used by Helmut Zepf, there is no defined maximum limit for processing cycles, provided that the functional integrity of the instrument is verified before each intervention. The use of damaged or worn products is strictly prohibited to avoid any risk of breakage or injury.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, headquartered in Seitingen-Oberflacht, Germany. This recognized manufacturer respects rigorous manufacturing standards for surgical instruments. The product is classified as a Class I medical device according to current regulations. The products are delivered non-sterile and must be prepared according to reprocessing protocols validated by the healthcare professional. Compliance with regulatory requirements ensures that the instrument meets the intended purposes for manual dental indication, subject to exclusive use by qualified healthcare professionals.


State of the art

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Specifications

Manufacturer Helmut Zepf
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