Double descaler instrument - Helmut Zepf (24.725.07) - Delynov
The Instrument à détartrer double - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.725.07.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf double-ended scaling instrument?
The Helmut Zepf double-ended scaling instrument, referenced under code 24.725.07, is a manual dental instrument designed for hygiene and prophylaxis procedures. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device features a double-ended configuration allowing for efficient handling during the removal of calcified deposits. As an instrument in the INSTRU category, it meets German manufacturing quality requirements for repeated use after reprocessing. Its rigid structure and metallic composition are specifically adapted to the mechanical stresses encountered during manual scaling in dental practices.
What are the clinical indications for this double scaler?
This instrument is indicated for the manual scaling of dental surfaces. It is primarily used in oral surgery and periodontology for the removal of supra-gingival calculus and extrinsic stains. The double scaler allows the practitioner to access different tooth surfaces for complete sanitization before more invasive interventions or during periodontal maintenance sessions. Its use is strictly reserved for qualified healthcare professionals, ensuring precise application on mineralized tissues without damaging adjacent structures, in accordance with its intended purpose as a manual dental instrument.
What are the technical characteristics of the 24.725.07 instrument?
The Helmut Zepf 24.725.07 instrument is characterized by its high-quality medical stainless steel design, providing the necessary resistance to sterilization cycles. It is a double-ended instrument, optimizing operative time by offering two active parts on a single handle. The cutting edges are designed to maintain their effectiveness during the excision of hard deposits. The manufacturer emphasizes the importance of checking for visible damage, such as cracks or defects on the cutting edges, before each use. This device is delivered non-sterile and requires a complete cleaning and sterilization protocol before its first use.
What are the contraindications for the use of this instrument?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during treatment, the procedure must be stopped immediately and necessary clinical measures must be taken. It is therefore imperative to validate the patient's history regarding metal allergies before any intervention. Furthermore, the use of instruments showing signs of wear, breakage, or defective cutting edges is prohibited.
What are the maintenance and reprocessing precautions?
As a non-resorbable and reusable instrument, the Helmut Zepf double scaler must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer specifies that due to the product design and materials used, there is no defined maximum limit of treatment cycles, provided that functional integrity is preserved. The practitioner must visually inspect the instrument to detect any trace of corrosion, crack, or deformation. Any damaged or worn product must never be used in order to guarantee patient safety and the effectiveness of the clinical procedure.
Who is the manufacturer and what standards are respected?
This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I medical device (Class Ir according to reprocessing details). The manufacturer complies with rigorous safety and quality protocols for manual instruments. Although specific CE marking is not detailed in the source data, the product complies with regulatory requirements for devices of its class intended for healthcare professionals. Traceability is ensured by the technical reference 24.725.07, allowing for precise identification of the model within the Helmut Zepf range.
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Specifications
| Manufacturer | Helmut Zepf |
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