Endodontic Set for Retrograde Technique - Helmut Zepf (24.725.00)
The Ensemble d'endodontie pour la technique rétrograde - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.725.00.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf endodontic set for retrograde technique?
The endodontic set for retrograde technique (reference 24.725.00) is a specialized instrumentation kit developed by Helmut Zepf Medizintechnik GmbH. This set is composed of manual dental instruments manufactured from high-quality medical stainless steel. It is specifically structured to meet the requirements of a-retro endodontic surgery. This medical device belongs to Class I according to current regulations. Its design aims to provide surgeons with a reliable solution for delicate interventions on the root apex, ensuring precise handling during the cleaning and canal preparation phases in a surgical environment.
What are the clinical indications?
This set is indicated for retrograde endodontic instrumentation during apical surgeries. Its use is recommended when conventional orthograde endodontic treatment is impossible, insufficient, or has failed. It is used by healthcare professionals to perform apex resections (apicoectomies) and for retrograde cavity preparation before filling. These instruments allow for direct intervention on the periapical area to eliminate infected tissue and hermetically seal the root canal at its terminal part, thus promoting bone healing and the preservation of the tooth on the dental arch.
What are the technical characteristics of this set?
The Helmut Zepf set is characterized by the exclusive use of medical stainless steel selected for its strength and compatibility with sterilization protocols. Listed under code 24.725.00, this surgical endo kit includes manual instruments whose geometry is adapted to the restricted access of the retrograde zone. The manufacturer states that due to the product design and materials used, there is no defined maximum limit for the number of processing cycles, although the service life depends on actual wear. Each instrument must undergo a rigorous inspection before use to detect any cracks or defects on the cutting edges.
What are the contraindications for use?
The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity to metals. Intolerance to medical stainless steel components in the patient can trigger adverse reactions during contact with the instrumentation. If a hypersensitivity reaction is observed during the intervention, the procedure must be immediately interrupted and the necessary medical measures must be taken. Furthermore, the use of these instruments is strictly reserved for qualified healthcare professionals. The use of instruments showing visible damage, such as breaks or excessive wear, is formally prohibited to guarantee patient safety.
What are the maintenance and sterilization precautions?
The instruments in this surgical endodontic set are delivered non-sterile and must undergo a full reprocessing cycle before the first use and after each subsequent use. The strict protocol includes cleaning, disinfection, and sterilization. It is crucial to check for the absence of visible damage such as cracks or defects on the working parts before each intervention. Never use damaged or worn products. Compatibility with other devices used simultaneously must also be verified beforehand. Compliance with these safety instructions ensures the longevity of the instrumentation and prevents the risks of cross-contamination in dental offices or hospital environments.
Who is the manufacturer and what standards are respected?
The official manufacturer of this set is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as a Class I manual dental instrument. The manufacturer complies with the regulatory requirements relating to medical devices to guarantee the safety and performance of its products. As a Class I device, it meets the rigorous manufacturing standards imposed by European regulations. Healthcare professionals can refer to the manufacturer's instructions for reprocessing and intended use, thus ensuring practice in accordance with current clinical standards in surgical endodontics.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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