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Syringe water for dental surgery - Helmut Zepf (19.762.00) - Delynov

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The Canule pour seringue à eau pour - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.762.00.
  • 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.

39.89 € 39.89 EUR 39.89 € Tax Included

39.89 € Tax Included

(39.89 € / Units)
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Instrument

What is the Helmut Zepf (19.762.00) water syringe cannula?

The Helmut Zepf water syringe cannula, referenced under code 19.762.00, is a manual dental instrument designed for oral care procedures. Manufactured in high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this cannula is an essential consumable for irrigation and cleaning during clinical interventions. As a Class I medical device, it meets safety requirements for professional use in dental practices. This device is delivered non-sterile and requires a rigorous preparation protocol before any commissioning, thus ensuring optimal hygiene for the patient and the practitioner.

What are the clinical indications for this instrument?

This manual dental instrument is primarily indicated for irrigation and rinsing during various dental procedures. Its use is reserved exclusively for qualified healthcare professionals. It serves as a distribution channel for water or rinsing solutions via a suitable syringe, allowing for the maintenance of a clean surgical field and the removal of debris during treatment. Its use is part of standard protocols for dental surgery and general practice where precise fluid management is necessary for the visibility and asepsis of the treated site.

What are the technical characteristics of the 19.762.00 cannula?

The Helmut Zepf (19.762.00) cannula is distinguished by its medical stainless steel construction, a material chosen for its durability and resistance to repeated processing cycles. Due to its robust design and the materials used, the manufacturer Helmut Zepf Medizintechnik GmbH specifies that there is no defined maximum limit for the number of reprocessing cycles, as long as the instrument does not show visible damage. Before each use, the practitioner must imperatively inspect the device to detect any potential cracks, breaks, or structural defects. The use of damaged or worn products is strictly prohibited to ensure the safety of care.

What are the possible contraindications and side effects?

The main contraindication for the use of this cannula is a known metal intolerance in the patient. Contact with medical stainless steel can, in certain cases, trigger a hypersensitivity reaction. If such an allergic reaction or intolerance occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to evaluate the patient's allergic history before use. Furthermore, the instrument must never be used if it shows signs of manifest wear or defects on the edges, in order to avoid any traumatic risk.

What are the maintenance and sterilization precautions?

In accordance with the manufacturer's instructions, all Helmut Zepf instruments must be cleaned, disinfected, and sterilized before their first use, as well as after each subsequent use. The reprocessing process must be complete and rigorous. It is crucial to clean each product before proceeding to sterilization to remove all organic residue. As the products are delivered non-sterile, strict compliance with these hygiene instructions is imperative to prevent cross-infections. The practitioner must also verify the compatibility of the cannula with other devices used during the procedure before any intervention.

Who is the manufacturer and what standards are met?

The cannula is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures the traceability and quality of its manual instruments intended for healthcare professionals. Compliance with the cleaning and sterilization protocols described by Helmut Zepf is essential to maintain the device's conformity throughout its useful life. As a Class I instrument, it meets the safety and performance standards required for non-invasive or low-risk medical devices used in a dental environment.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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