Fine Brush - Helmut Zepf (19.199.12) - Delynov becomes Fine Brush for
The Pinceau fin - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.199.12.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf fine brush (19.199.12)?
The fine brush developed by Helmut Zepf Medizintechnik GmbH is a manual instrument specifically designed for restorative dentistry and oral surgery procedures. Referenced under code 19.199.12, this device belongs to the category of modeling instruments. Its structure allows for delicate manipulation of restorative materials. As a dental application brush, it is used by practitioners to structure resins and composites with great finesse. This product is manufactured according to Helmut Zepf quality standards, guaranteeing a tool adapted to the clinical requirements of dental practices and implant surgery centers.
What are the clinical indications for this brush?
The Helmut Zepf fine brush is indicated for all procedures requiring a precise dental modeling brush. Its main use concerns the application and shaping of aesthetic restorative materials. In clinical practice, it serves as a composite brush to smooth surfaces and adjust the contours of direct or indirect restorations. It is particularly useful in reconstruction protocols where the resin modeling brush allows for obtaining optimal occlusal or proximal morphology. This manual instrument is intended exclusively for professional use by qualified practitioners in dental and implant surgery.
What are the technical characteristics of this instrument?
The Helmut Zepf fine brush, bearing reference 19.199.12, is a non-sterile manual instrument. It is designed from medical stainless steel for the structural parts, a material recognized for its resistance to cleaning and sterilization cycles. This resin application brush is developed to offer a precise tactile response when working with viscous materials. Due to its design and the materials used, the manufacturer Helmut Zepf Medizintechnik GmbH specifies that there is no defined maximum limit for processing cycles, provided that the visual integrity of the instrument is preserved before each use.
What are the contraindications for the use of this brush?
The main contraindication related to the use of this Helmut Zepf instrument is known hypersensitivity or intolerance to metals, particularly to the medical stainless steel composing the instrument. If an allergic reaction or intolerance occurs in the patient during contact, the clinical procedure must be immediately interrupted and necessary medical measures must be taken. It is the responsibility of the practitioner to check the patient's history of metal allergies before any intervention. Furthermore, the use of the instrument is prohibited if visible damage such as cracks, breaks, or defects are found on the product.
What are the maintenance and reprocessing precautions?
Helmut Zepf Medizintechnik GmbH products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is crucial to inspect the fine brush for any signs of wear, corrosion, or deformation before each cycle. The use of damaged or worn products is strictly prohibited to guarantee patient safety and treatment efficacy. The reprocessing process must follow standard hospital or dental office sterilization protocols. Compatibility with other cleaning products must also be verified beforehand by the healthcare professional.
Who is the manufacturer and what standards are respected?
The official manufacturer of this brush is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to the reference text). Compliance with manufacturing standards guarantees that the instrument meets the safety requirements for manual medical devices. As a Class I product, it follows the regulatory conformity assessment procedures applicable to reusable dental instruments. Maintaining compliance depends on rigorous adherence to the cleaning and sterilization instructions provided by the manufacturer to ensure the longevity of the instrument in the surgical environment.
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Specifications
| Manufacturer | Helmut Zepf |
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