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Claw forceps 1x2 - Helmut Zepf (22.408.11) - Delynov

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The Pince à griffes 1x2 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 22.408.11.
  • Reserved for healthcare professionals. Read instructions carefully before use.

fabricant : HELMUT ZEPF Medizintechnik Gmbh , Obere Hauptstraße 16-22, D- 78606 Seitingen-Oberflacht BUT PRÉVU / INDICATION Instrument dentaire manuel  Les effets secondaires indésirables l'intolérance aux métaux chez le patient peut résulter d'un contact avec l'instrument, qui est en acier inoxydable médical une réaction d'hypersensibilité était toujours déclenchée devenir. la procédure doit être arrêtée si une telle réaction se produit et les mesures nécessaires sont prises en conséquence. consignes d'utilisation et de sécurité tous les instruments doivent être nettoyés avant d'être utilisés pour la première fois et compléter avant toute utilisation ultérieure nettoyé, désinfecté et stérilisé ! il est très important de nettoyer chaque produit avant utilisation dommages et usures visibles, par ex. b. fissures, cassures ou des défauts sur les arêtes de coupe. n'utilisez jamais de produits endommagés ou usés. les produits de helmut zepf medizintechnik gmbh sont livrés non stériles. les produits doivent être à l'avance nettoyé et stérilisé. la compatibilité aussi les autres produits doivent être vérifiés au préalable. retraitement en raison de la conception du produit, des matériaux utilisés et il ne peut y avoir de limite maximale définie pour l'utilisation prévue des cycles de traitement réalisables peuvent être déterminés.réservé aux professionnels de santé.

41.34 € 41.34 EUR 41.34 € Tax Included

41.34 € Tax Included

(41.34 € / Units)
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Instrument

What is the Helmut Zepf 1x2 tissue forceps (22.408.11)?

The Helmut Zepf 1x2 tissue forceps, referenced under code 22.408.11, is a high-precision manual dental instrument designed for oral surgery procedures and Guided Bone Regeneration (GBR). Manufactured from premium medical grade stainless steel by Helmut Zepf Medizintechnik GmbH, these forceps are distinguished by their 1x2 teeth configuration, allowing for a secure grip of tissues or surgical materials. This device is categorized as a Class I instrument, ensuring compliance with regulatory requirements for non-invasive or reusable medical devices after processing. Its robust design ensures reliable handling during delicate interventions in the dental office.

What are the clinical indications for this instrument?

This manual dental instrument is specifically indicated for oral surgery procedures requiring precise manipulation of soft tissues or regeneration membranes. The Helmut Zepf 1x2 tissue forceps is an essential tool in implantology and periodontology, particularly during GBR phases. It allows the practitioner to firmly hold tissues without excessive slippage thanks to its toothed structure. Its use is strictly reserved for qualified healthcare professionals. The manufacturer emphasizes that the instrument must be used in accordance with its intended use as a manual gripping device to guarantee clinical efficacy and patient safety during surgical protocols.

What are the technical characteristics of the 22.408.11 forceps?

The Helmut Zepf forceps (22.408.11) is designed in medical grade stainless steel, a material chosen for its mechanical resistance and its ability to undergo repeated sterilization cycles. Its 1x2 teeth technical configuration offers an optimal balance between holding force and reduced tissue trauma. As a Class I device, it meets the rigorous manufacturing standards of Helmut Zepf Medizintechnik GmbH. The instrument is delivered non-sterile and requires rigorous preparation before any use. Its ergonomic design allows for a stable grip, facilitating complex surgical maneuvers in confined areas, while guaranteeing durability in line with the expectations of dental surgeons.

What are the contraindications for the use of this instrument?

The main contraindication related to the use of these medical grade stainless steel forceps lies in patient hypersensitivity or intolerance to metals. A hypersensitivity reaction can be triggered during direct contact with the instrument. The manufacturer, Helmut Zepf, specifies that if such a reaction occurs, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, it is formally contraindicated to use the instrument if it shows visible damage or wear, such as cracks, breaks, or defects on the cutting edges, as this could compromise patient safety and the outcome of the intervention.

What are the maintenance and sterilization precautions?

Like all instruments from the Helmut Zepf brand, the tissue forceps must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to check for the absence of visible damage before each handling. The reprocessing process must be complete to guarantee asepsis. Due to the quality of the materials used and the design of the instrument, there is no defined maximum limit for processing cycles, as long as the physical integrity of the forceps is preserved. The use of damaged or worn products is strictly prohibited to avoid any risk of surgical complication or cross-contamination.

Who is the manufacturer and what standards are met?

The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. Although specific CE marking is not detailed in the provided source data, the product complies with manufacturing standards for manual dental instruments in medical grade stainless steel. Compatibility with other products used during the intervention must be verified beforehand by the healthcare professional. Helmut Zepf is recognized for its expertise in the design of durable surgical tools intended exclusively for experts in the dental and maxillofacial surgery sector.


State of the art

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

Specifications

Manufacturer Helmut Zepf
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