Crown Removal Porcelain Pliers - Helmut Zepf (19.274.00)
The Pince à enlever les couronnes en porcelaine - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.274.00.
- Reserved for healthcare professionals. Read instructions carefully before use.
What are the Helmut Zepf crown removing pliers?
The Helmut Zepf crown removing pliers, referenced under code 19.274.00, are a manual instrument specifically designed for the manipulation and removal of fixed dental prostheses, particularly those made of porcelain. Manufactured by Helmut Zepf Medizintechnik GmbH, these pliers are designed in high-quality medical stainless steel to meet the requirements of oral surgery and prosthetics. Their structure is designed to offer a firm grip on ceramic surfaces, allowing the practitioner to exert the forces necessary for the disinsertion of the crown without compromising the integrity of the surrounding tissues or the underlying pillar.
What are the clinical indications for this instrument?
This instrument is indicated for all procedures requiring the removal of definitive or temporary prosthetic crowns, particularly in porcelain. In clinical practice, it is used during the removal of defective prostheses, the treatment of secondary caries under the crown, or during the re-evaluation of implant pillars. The crown removing pliers are an indispensable tool in prosthetics and surgery for accessing dental structures or implant components covered by a fixed restoration. Its use is strictly reserved for qualified healthcare professionals within the framework of dental and surgical care in a practice or hospital environment.
What are the technical characteristics of reference 19.274.00?
The Helmut Zepf 19.274.00 pliers are characterized by their manufacture in medical stainless steel, guaranteeing optimal resistance to repeated sterilization cycles. As a manual instrument, it does not include an automated mechanism, leaving the practitioner in total control of the applied force. The manufacturer specifies that due to its design and the materials used, there is no defined maximum limit for the number of processing cycles achievable, although the instrument must be inspected before each use to detect possible visible damage such as cracks or defects on the active parts. It is delivered non-sterile and must follow a complete cleaning and sterilization protocol before the first use.
What are the contraindications for the use of these pliers?
The main contraindication related to the use of this instrument is hypersensitivity or known intolerance of the patient to metals, and more specifically to the components of medical stainless steel. The manufacturer, Helmut Zepf Medizintechnik GmbH, warns that a hypersensitivity reaction can be triggered upon contact of the instrument with the tissues. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and the necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any manipulation with this metallic instrument.
What maintenance and safety precautions should be observed?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use, as well as after each subsequent use. It is crucial to perform a complete cleaning to remove all residues before the sterilization cycle. Before each intervention, the practitioner must visually inspect the pliers to identify any trace of wear, corrosion, cracks, or breaks. The use of a damaged instrument or one presenting defects on the edges is prohibited. Furthermore, compatibility with other products used during the care session must be verified beforehand to guarantee patient safety and the effectiveness of the surgical procedure.
Who is the manufacturer and what standards are respected?
The device is manufactured by Helmut Zepf Medizintechnik GmbH, a company located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device according to the regulations in force. The manufacturer respects rigorous manufacturing protocols to ensure the compliance of its manual instruments with the requirements of the dental sector. The products are delivered non-sterile and require systematic reprocessing by healthcare professionals. Following the instructions provided by Helmut Zepf regarding cleaning and sterilization is essential to maintain the compliance of the instrument and ensure clinical safety during crown removal procedures.
State of the art
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Specifications
| Manufacturer | Helmut Zepf |
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