Flexible Insert - Helmut Zepf (19.201.21)
The Insert souple - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.201.21.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf soft insert (19.201.21)?
The Helmut Zepf soft insert, identified under technical reference 19.201.21, is a consumable accessory intended for use with the brand's surgical instrumentation. This type of component is designed to provide a flexible interface between the main instrument and the tissues or structures being manipulated. Its specific design by Helmut Zepf Medizintechnik GmbH guarantees optimal compatibility with devices in the corresponding range, thus maintaining the operational integrity of the instrument during oral surgery procedures.
What are the clinical indications for this insert?
The use of this soft insert is primarily indicated in the context of implant, periodontal, or general oral surgeries. It is often used when soft tissue protection or precise adaptation to dental morphology is required. As an element of the CONSO category, it is used to complement the action of more complex instruments, facilitating the practitioner's technical movements during procedures requiring contact flexibility or specific pressure absorption.
What are the technical characteristics of this accessory?
The soft insert is defined by its catalog reference 19.201.21. Although the precise materials are not detailed in the raw technical sheet, this type of Helmut Zepf component is developed to meet the flexibility and resistance requirements necessary in a clinical environment. Its geometry is specifically adjusted for precise mounting on compatible instruments, ensuring stability during the intervention without compromising the overall maneuverability of the surgical device.
What are the contraindications for the use of this insert?
Specific contraindications for the soft insert 19.201.21 are not exhaustively listed in the provided data. However, generally in oral surgery, the use of this accessory is contraindicated in cases of known hypersensitivity to the device's constituent materials. The insert should also not be used if it shows visible signs of degradation or if compatibility with the carrier instrument is not strictly verified according to the manufacturer's recommendations.
What are the precautions for use and maintenance?
As a product in the consumable category, precautions for use include systematic verification of the insert's condition before each intervention. The flexibility of the element must meet expectations to ensure patient safety and the effectiveness of the surgical movement. Although resorption modalities do not apply here, the practitioner must refer to the instructions from Helmut Zepf Medizintechnik GmbH regarding cleaning, sterilization, or the potential single-use nature of the component.
Who is the manufacturer and what standards are met?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the field of dental and surgical instrumentation. Regarding regulatory standards, the class and CE marking are not specified in the current source data. It is therefore imperative for the dental surgeon or implantologist to consult the instructions for use attached to the product or to contact the manufacturer directly to obtain certificates of conformity and details relating to current ISO standards.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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