Oral Surgery and Implantology Probe Helmut Zepf (24.102.23) - Delynov
The sonde de chirurgie orale et implantologie Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.102.23.
- 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 is the Helmut Zepf oral surgery and implantology probe (24.102.23)?
The Helmut Zepf oral surgery and implantology probe (reference 24.102.23) is a high-precision manual dental instrument designed for interventions in surgical and implant environments. Manufactured from superior quality medical stainless steel by Helmut Zepf Medizintechnik GmbH, this instrument belongs to the category of reusable consumables. It is distinguished by its robustness and ergonomic design adapted to the requirements of oral surgery. This medical device is classified as a Class I instrument according to current regulations. It is delivered in a non-sterile state, requiring complete processing by healthcare personnel before any first clinical use.
What are the clinical indications for this Helmut Zepf instrument?
This Helmut Zepf manual dental instrument is specifically indicated for oral surgery and implantology procedures. Its intended purpose is to assist the practitioner during examination or intervention phases within the oral cavity. As a precision instrument, it allows for fine manipulation and precise diagnosis of tissues or implant sites. The use of this probe is strictly reserved for qualified healthcare professionals, such as dental surgeons and implantologists, thus guaranteeing a secure application in compliance with standard clinical protocols in a dental care environment.
What are the technical characteristics of the 24.102.23 probe?
The Helmut Zepf 24.102.23 probe is characterized by its integral manufacture in medical stainless steel, a material chosen for its corrosion resistance and durability through reprocessing cycles. Unlike sutures, this instrument does not have a needle or thread, but a rigid structure designed for exploration and measurement in surgery. An important technical feature lies in the absence of a defined maximum limit for achievable processing cycles, subject to the maintenance of the object's physical integrity. Its design allows for thorough cleaning, ensuring impeccable hygiene between each patient after appropriate sterilization.
What are the contraindications for the use of this instrument?
The main contraindication for the use of this medical stainless steel probe concerns patients with a known intolerance to metals. Contact with the instrument can potentially trigger a hypersensitivity reaction in these individuals. The manufacturer specifies that if such an allergic reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, it is strictly forbidden to use the instrument if it shows visible damage, such as cracks, breaks, or defects on the active parts, in order to prevent any risk of injury or complication for the patient.
What are the maintenance and reprocessing precautions?
Reprocessing the Helmut Zepf probe is a critical step for care safety. All instruments must imperatively be cleaned, disinfected, and sterilized before their first use and after each subsequent use. The manufacturer emphasizes that it is crucial to clean each product before proceeding with sterilization. Before each use, the professional must inspect the instrument to detect any potential wear or visible damage (cracks, edge defects). Due to its robust design and the materials used, the number of sterilization cycles is not limited by a fixed figure but depends on the physical condition of the instrument. The use of damaged or worn products is strictly prohibited.
Who is the manufacturer and what standards are respected?
This probe is produced by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. The device complies with medical device regulations as a Class I product. It is identified under the reference code 24.102.23. The manufacturer insists on rigorous compliance with instructions for use and safety, notably the prior verification of compatibility with other products used during the intervention. As a Class I instrument, it meets the quality and safety requirements imposed for reusable manual dental instruments, guaranteeing optimal reliability for dental health professionals.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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