Prichard Periosteal Elevator - Helmut Zepf (24.751.126) - Delynov
The Rugine pour Prichard - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 24.751.126.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Prichard periosteal elevator?
The Prichard periosteal elevator, referenced under code 24.751.126 by the manufacturer Helmut Zepf Medizintechnik GmbH, is a manual instrument specific to oral surgery. This device is designed in medical stainless steel, a standard material for surgical instrumentation ensuring the necessary resistance for clinical procedures. As an instrument in the CONSO category at Delynov, it is part of a range of devices intended for healthcare professionals requiring reliable tools for the manipulation of soft tissues and the periosteum. Its structure is adapted to the requirements of daily practice in dental offices or hospital environments.
What are the clinical indications for this instrument?
The intended use for this Prichard periosteal elevator is that of a manual dental instrument intended for oral surgery procedures. It is primarily indicated for mucoperiosteal detachment, allowing for the delicate separation of the periosteum from the bone surface. This action is fundamental during the creation of flaps for periodontology procedures, pre-implant surgery, or complex extractions. The instrument allows for optimal visibility of the surgical field by retracting soft tissues in a controlled manner. Its use is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.
What are the technical characteristics of the 24.751.126 periosteal elevator?
The Prichard periosteal elevator developed by Helmut Zepf is characterized by its manufacture in high-quality medical stainless steel. This material is chosen for its ability to withstand repeated cycles of cleaning, disinfection, and sterilization. The device is delivered non-sterile and must imperatively undergo full reprocessing before its first use and after each subsequent use. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit for the number of processing cycles, as long as the instrument does not show visible damage such as cracks or defects on the active parts.
What are the contraindications for the use of this instrument?
The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Contact between the stainless steel instrument and an allergic patient can trigger an adverse reaction. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to check the patient's allergic history before any manipulation. Furthermore, the use of the instrument is contraindicated if it shows obvious signs of wear, breaks, or damaged cutting edges.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before their first use and between each patient. It is imperative to check the condition of each product before use to detect any visible damage such as cracks or deformations. Never use damaged or worn products, as this could compromise the safety of the surgical act. Reprocessing must follow standard hospital or dental office sterilization protocols. Compatibility with other products used during the procedure must also be verified beforehand by the practitioner.
Who is the manufacturer and what standards are respected?
This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. The device is classified as a Class I instrument according to current regulations. As the official manufacturer, Helmut Zepf guarantees that its products meet the safety requirements for manual dental instruments. Compliance with cleaning and sterilization instructions is essential to maintain the conformity of the device throughout its useful life. This equipment is exclusively reserved for professional use by healthcare practitioners trained in dental surgical techniques.
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Specifications
| Manufacturer | Helmut Zepf |
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