Removable Figure 222 Dental Form - Helmut Zepf (14.222.00) - Delynov
The DAVIER FORME AMOVIBLE FIGURE 222 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 14.222.00.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf figure 222 extraction forceps?
The Helmut Zepf figure 222 extraction forceps, referenced under code 14.222.00 at Delynov, is a manual instrument specific to dental surgery. This device is manufactured from medical grade stainless steel, a material selected for its resistance and compatibility with sterilization processes. Its removable form structure is designed to meet the requirements of practitioners during surgical acts. As an instrument from the Helmut Zepf brand, it benefits from the expertise of a recognized manufacturer in the field of odontological instrumentation. This dental forceps is classified as a Class I medical device, intended exclusively for professional use by qualified health practitioners.
What are the clinical indications?
This molar extraction forceps is indicated for simple or complex exodontia procedures in oral surgery. Its intended purpose is to serve as a manual instrument for the manipulation and extraction of teeth. It is used by dental surgeons and implantologists during alveolar site preparation phases or during the management of compromised teeth. The official indication provided by the manufacturer Helmut Zepf Medizintechnik GmbH specifies that it is a manual dental instrument. Its use is strictly reserved for healthcare professionals trained in dental surgical techniques, thus ensuring application in accordance with current clinical protocols.
What are the technical characteristics?
The Helmut Zepf extraction forceps (reference 14.222.00) is distinguished by its medical stainless steel design, ensuring durability through reprocessing cycles. Figure 222 corresponds to a specific geometry adapted to dental anatomy to facilitate grip during extraction. The device is delivered non-sterile, which requires a strict preparation protocol before the first use. The product design and the materials used do not allow for a defined maximum limit of treatment cycles, although visible wear must be monitored. Each instrument must undergo a meticulous inspection to detect any cracks or defects on the edges before any intervention.
What are the contraindications for use?
The main contraindication related to the use of this dental forceps is the patient's known hypersensitivity or intolerance to metals, and more particularly to the components of medical stainless steel. The manufacturer warns that a hypersensitivity reaction may be triggered upon contact with the instrument. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before use. Additionally, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the active parts.
What are the maintenance and reprocessing precautions?
The Helmut Zepf extraction forceps is a reusable instrument that requires rigorous maintenance. According to safety instructions, all instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to perform a complete cleaning before sterilization to ensure the effectiveness of the process. The practitioner must check for the absence of visible damage and wear, such as cracks or defects on the cutting edges, before each use. The use of damaged or worn products is prohibited. Due to its robust stainless steel design, there is no predefined limit on the number of sterilization cycles, subject to maintaining the physical integrity of the instrument.
Who is the manufacturer and what standards are met?
The official manufacturer of this device is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This forceps is a Class I medical device, complying with regulatory requirements for manual dental instruments. The manufacturer emphasizes that its products are delivered non-sterile and must undergo a full cycle of cleaning and sterilization before use. Traceability and manufacturing quality are ensured by the expertise of Helmut Zepf, an established player in the production of surgical instruments. Compliance with reprocessing protocols and exclusive use by healthcare professionals are essential conditions to guarantee the safety and performance of the device.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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