Helmut Zepf Graduated Periodontal Probe for Dental Surgery
The Sonde parodontale graduée Helmut Zepf pour is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- 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 graduated periodontal probe?
The Helmut Zepf graduated periodontal probe is a high-precision manual dental instrument designed for clinical examination in periodontology. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, it is presented as a robust and durable tool. This device belongs to the consumables category (CONSO) and is classified as a Class I instrument according to current regulations. Its stainless steel design provides the rigidity necessary for exploring periodontal pockets while ensuring standard biocompatibility for oral tissues. It is delivered non-sterile and requires a complete preparation protocol before any surgical intervention or clinical examination.
What are the clinical indications for this instrument?
The intended use of this Helmut Zepf manual dental instrument is the evaluation and diagnosis of periodontal tissues. As a graduated measuring instrument, it allows the practitioner to quantify pocket depth, evaluate the epithelial attachment level, and detect root surface irregularities. Its use is strictly reserved for healthcare professionals qualified in dental and oral surgery. The instrument is essential for establishing an accurate periodontal diagnosis, monitoring the progression of gingival pathologies, and verifying the effectiveness of scaling and root planing treatments during maintenance phases.
What are the technical and maintenance characteristics?
This probe is distinguished by its manufacture in high-quality medical stainless steel. The manufacturer, Helmut Zepf Medizintechnik GmbH, emphasizes that the product does not have a defined maximum limit of processing cycles, with the service life depending on actual wear and visible damage. Before each use, the instrument must imperatively be cleaned, disinfected, and sterilized. Rigorous visual inspection is necessary to identify any cracks, breaks, or defects on the edges and graduations. The use of damaged or worn products is prohibited to ensure patient safety and the accuracy of clinical measurements.
What are the contraindications for the use of this probe?
The main contraindication related to the use of this medical stainless steel instrument is metal intolerance in the patient. A hypersensitivity reaction may be triggered upon contact with the instrument. If such an intolerance or hypersensitivity reaction occurs during the examination, the procedure must be stopped immediately and the necessary medical measures must be taken accordingly. It is therefore recommended to question the patient about their history of metal allergies before any manipulation. Additionally, use is contraindicated if the instrument shows visible signs of degradation such as cracks or corrosion.
What are the precautions for use and reprocessing?
All Helmut Zepf instruments must be cleaned before their first use, then fully cleaned, disinfected, and sterilized before each subsequent use. It is crucial to check compatibility with other products used during the care protocol. Due to its metallic design, reprocessing must follow standard hospital or dental office sterilization protocols. The professional must remain vigilant regarding wear: any defect on the graduations or the structural integrity of the probe requires its immediate withdrawal from clinical use. Strict compliance with these safety instructions ensures the longevity of the instrument and the aseptic safety of the patient.
Who is the manufacturer and what standards are met?
This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device complies with Class I for manual dental instruments. The manufacturer imposes strict guidelines regarding cleaning and sterilization prior to any intervention. As a Class I product, it meets the safety and performance requirements for non-invasive or short-term invasive devices. Healthcare professionals must refer to the manufacturer's instructions to ensure continued product compliance throughout its life cycle, particularly regarding reprocessing procedures and surface condition verification.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |