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Short Screwdriver - Helmut Zepf (47.832.01) - Delynov

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The Tournevis court - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 47.832.01.
  • Reserved for healthcare professionals. Read instructions carefully before use.

64.83 € 64.83 EUR 64.83 € Tax Included

64.83 € Tax Included

(64.83 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf short screwdriver?

The short screwdriver, referenced under code 47.832.01, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. It is specifically designed for practitioners specializing in oral surgery and implantology. Its structure is developed in medical stainless steel, ensuring compatibility with rigorous sterilization protocols. As a Class I device, it meets the quality requirements for non-invasive or invasive instruments for temporary use. This screwdriver is distinguished by its compactness, allowing for easy handling in clinical environments where workspace is limited, thus facilitating the screwing of fixation devices or implant components.

What are the clinical indications for this instrument?

This Helmut Zepf manual screwdriver is indicated for various oral surgery procedures, particularly within the framework of guided bone regeneration (GBR) and implantology. It is used for the placement, tightening, or removal of fixation screws, abutments, or healing screws. Its short shape is particularly suited to the posterior sectors of the oral cavity, where the patient's mouth opening or the proximity of soft tissues limits the use of longer instruments. The use of this instrument is strictly reserved for qualified healthcare professionals, ensuring application in accordance with current clinical standards.

What are the technical characteristics of the 47.832.01 screwdriver?

The Helmut Zepf screwdriver (ref. 47.832.01) is a one-piece or assembled manual instrument, designed to offer a tightening torque controlled by the practitioner. Manufactured from medical stainless steel, it exhibits high resistance to corrosion and repeated reprocessing cycles. It is delivered non-sterile and must imperatively undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each intervention. Its short ergonomic design aims to optimize tactile control during critical screwing phases in implant surgery, while ensuring compatibility with other products in the manufacturer's surgical range.

What are the contraindications for the use of this device?

The main contraindication related to the use of this medical stainless steel screwdriver is the patient's known hypersensitivity or intolerance to metals. If an allergic reaction or hypersensitivity reaction is triggered upon contact with the instrument, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the active parts. It is imperative to inspect the instrument before each use to guarantee patient safety and the effectiveness of the surgical procedure.

What are the maintenance and reprocessing precautions?

Like any Helmut Zepf instrument, this screwdriver must be cleaned, disinfected, and sterilized before each use. Due to its design and the materials used, there is no defined maximum limit for processing cycles, provided that the instrument shows no functional wear. The practitioner must check for the absence of visible damage before any intervention. Damaged or worn products must never be used. The reprocessing process must scrupulously follow the manufacturer's safety instructions to maintain the integrity of the medical stainless steel and prevent any risk of cross-contamination in the dental office or hospital environment.

Who is the manufacturer and what standards are respected?

The short screwdriver is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the conformity of its products with safety and performance requirements for manual dental instruments. Traceability is ensured by the technical reference 47.832.01. Healthcare professionals can refer to the manufacturer's instructions (MDC0483) for details regarding intended use, warnings, and cleaning protocols. The quality of the medical steel used highlights Helmut Zepf's commitment to providing reliable instruments for specialized surgery.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Helmut Zepf
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