Points for Miller - Helmut Zepf (19.272.02) - Delynov becomes Points for Miller - Helmut Zepf (19.272.02) - Delynov.
The Pointes pour Miller - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.272.02.
- 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.
What are the tips for Miller Helmut Zepf (19.272.02)?
The tips for Miller, referenced under code 19.272.02, are manual dental instruments designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This Class I medical device is manufactured from medical-grade stainless steel, ensuring robustness suited to the requirements of dental surgery. As an instrument in the consumable (CONSO) category, this product is delivered non-sterile by Helmut Zepf. It imperatively requires a complete cleaning, disinfection, and sterilization protocol before its first use, as well as between each patient. Its specific metallic design is intended to meet the precise needs of practitioners in dental offices or hospital environments for targeted manual interventions.
What are the clinical indications for this instrument?
The intended use for these tips for Miller Helmut Zepf is that of a manual dental instrument. They are indicated for oral and dental surgery interventions requiring precision instrumentation. This device is exclusively reserved for qualified healthcare professionals. The manufacturer specifies that the instrument must be inspected before each use to detect any potential damage or visible wear, such as cracks, breaks, or defects on the cutting edges. The use of damaged products is strictly prohibited to guarantee the safety of care and the effectiveness of the clinical procedure undertaken by the dental surgeon or implantologist.
What are the technical characteristics of reference 19.272.02?
Technical reference 19.272.02 corresponds to a manual instrument made of medical stainless steel developed by Helmut Zepf Medizintechnik GmbH. This material was selected for its durability and its ability to undergo repeated processing cycles. Due to the specific design of the product and the materials used, the manufacturer indicates that there is no defined maximum limit for the number of reprocessing cycles achievable, provided that the physical integrity of the instrument is preserved. Before any use, compatibility with other products must be verified by the practitioner. The absence of visible damage on surfaces and edges is an essential technical criterion for maintaining the instrument's performance during operative acts.
What are the contraindications for the use of these tips?
The main contraindication related to the use of this medical stainless steel instrument concerns metal intolerance. Contact with the instrument may lead to a hypersensitivity reaction or intolerance in patients sensitive to the alloy components. If such a reaction occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures must be taken accordingly. It is therefore recommended to evaluate the patient's history of metal allergies before any manipulation. Furthermore, use is contraindicated if the instrument shows signs of wear, corrosion, or structural deformation compromising its safety of use.
What are the maintenance and sterilization precautions?
As Helmut Zepf products are delivered non-sterile, a strict reprocessing protocol is mandatory. All instruments must be cleaned, disinfected, and sterilized before the first use, and then after each subsequent use. Cleaning must be thorough to eliminate all organic residue. It is crucial to check for the absence of cracks or defects on the cutting edges before proceeding with sterilization. The manufacturer emphasizes that it is very important to clean each product individually. The use of worn instruments or those with visible defects is dangerous and prohibited. Compliance with these safety instructions ensures the longevity of the device and the protection of the patient against risks of cross-contamination.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device, in accordance with the regulations in force for manual dental instruments. Although the specific CE marking is not detailed in the provided sources, the manufacturer complies with manufacturing requirements for stainless steel medical devices. Traceability is ensured by reference 19.272.02. This equipment is strictly reserved for professional use by trained healthcare practitioners. The manufacturer insists on the final user's responsibility regarding the verification of the instrument's condition and the implementation of appropriate sterilization processes before any clinical act.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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