Miller Crown Remover - Helmut Zepf (19.272.10) - Delynov
The Arrache-couronnes Miller - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.272.10.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Miller crown remover?
The Miller crown remover, bearing reference 19.272.10, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical-grade stainless steel, this device is intended for the removal of fixed prosthetic elements. Its structure is specifically studied to meet the requirements of daily practice in dental offices and oral surgery. As a non-sterile instrument upon delivery, it requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient, thus ensuring optimal safety of use in the clinical setting.
What are the clinical indications for this instrument?
This instrument is indicated for the removal of crowns and bridges during prosthetic repair procedures or endodontic treatments requiring access to the underlying tooth structure. The Helmut Zepf Miller crown remover allows the practitioner to exert a controlled mechanical action to break the cement seal. Its use occurs mainly in restorative dentistry and surgery to free dental or implant abutments. The manufacturer specifies that it is a manual dental instrument reserved exclusively for qualified healthcare professionals, to be used according to the state of the art of the profession.
What are the technical characteristics of the Miller crown remover?
The Miller crown remover (reference 19.272.10) is distinguished by its manufacture in high-quality medical stainless steel, ensuring the robustness necessary for the tensile forces exerted. This Helmut Zepf device is classified as a Class I instrument according to current regulations. Its design allows for complete reprocessing without a defined maximum limit of cycles, provided there is an absence of visible damage. Before each intervention, the practitioner must imperatively inspect the instrument to detect any cracks, breaks, or defects on the active parts, as the use of damaged or worn products is strictly prohibited to maintain the integrity of care.
What are the contraindications for the use of this device?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance of the patient to metals. As the instrument consists of medical stainless steel, contact can trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the procedure, the intervention must be immediately interrupted and the necessary medical measures must be taken. It is therefore crucial to evaluate the patient's anamnesis regarding allergies to metallic components before any manipulation with this manual instrument.
What are the maintenance and reprocessing precautions?
Reprocessing of the Miller crown remover follows a rigorous protocol. As Helmut Zepf products are delivered non-sterile, a complete cleaning, disinfection, and sterilization cycle is mandatory before the first use. Due to the design and materials used, there is no predefined maximum limit of treatment cycles, but the longevity of the instrument depends on systematic inspection before use. Any sign of wear, corrosion, or deformation must lead to the immediate disposal of the device. Compatibility with other cleaning and sterilization products must also be verified beforehand by the professional.
Who is the manufacturer and what standards are respected?
The Miller crown remover is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to certain reprocessing nomenclatures). Compliance with manufacturing standards is based on the use of medical stainless steel meeting safety requirements for manual instruments. The manufacturing process follows directives relating to medical devices, ensuring that each instrument meets the quality standards required for professional use in a clinical environment. The manufacturer emphasizes that the use of this instrument is strictly reserved for trained healthcare professionals.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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