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ApplicatorApplicator for implantology and dental surgery equipment - Helmut Zepf (19.714.21) - Delynov

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The ApplicateurApplicateur pour matériel d'implantologie et chirurgie dentaire - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.714.21.
  • Reserved for healthcare professionals. Read instructions carefully before use.

74.88 € 74.88 EUR 74.88 € Tax Included

74.88 € Tax Included

(74.88 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf (19.714.21) applicator?

The Helmut Zepf applicator, referenced under code 19.714.21, is a manual dental instrument specifically developed for the needs of implant and oral surgery. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is designed in high-quality medical stainless steel, ensuring structural resistance adapted to clinical requirements. As a Class I instrument, it is intended for use by qualified healthcare professionals. Its structure is optimized for the manipulation of various materials, offering a rigid and durable interface between the practitioner's hand and the surgical site, while respecting German manufacturing standards.

What are the clinical indications for this instrument?

This instrument is indicated as a manual dental instrument for procedures requiring precise application of materials. In practice, it is used as an implantology material applicator for the deposition of bone substitutes or as a biomaterial placement instrument during guided bone regeneration (GBR) or sinus lift surgeries. Its role is to ensure the controlled transfer and placement of surgical components within the oral cavity. It is also suitable for implant placement procedures where instrumental manipulation is required to adjust or position prosthetic elements or temporary surgical components.

What are the technical characteristics of this applicator?

The Helmut Zepf (19.714.21) applicator is characterized by its full medical stainless steel composition, a material chosen for its biocompatibility and its ability to undergo repeated reprocessing cycles. It is a non-sterile device upon delivery, requiring a complete cleaning, disinfection, and sterilization protocol before the first use and after each subsequent use. Due to its robust design and the materials used, the manufacturer has not defined a maximum limit for treatment cycles, although a visual inspection to detect any cracks, breaks, or defects on the edges is imperative before each procedure.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns patients with a known intolerance or hypersensitivity to metals. Contact with medical stainless steel can trigger a hypersensitivity reaction in these individuals. If such a reaction occurs during the procedure, the process must be stopped immediately and the necessary clinical measures must be taken. Furthermore, the use of the instrument is strictly prohibited if it shows visible damage, such as cracks or excessive wear, to ensure patient safety and the effectiveness of the surgical act.

What are the maintenance and reprocessing precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use. The reprocessing process must be complete before each subsequent use. It is crucial to check for the absence of visible damage such as breaks or defects on the cutting edges before any manipulation. The use of damaged or worn products is prohibited. Since these devices are delivered non-sterile, compliance with the sterilization protocols in force in dental surgery practices is mandatory. Compatibility with other products used simultaneously must also be verified beforehand by the practitioner.

Who is the manufacturer and what standards are respected?

This applicator is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its products with safety and performance requirements for manual instruments. As a Class I device, it meets European manufacturing standards for reusable instruments. The use of this implant placement instrument is strictly reserved for trained healthcare professionals, thus ensuring an application consistent with established scientific data and the safety instructions provided by Helmut Zepf.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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