Heidbrink. Fragment Debrider - Helmut Zepf (17.051.03) - Delynov
The Heidbrink. Décortiqueur à Fragments - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 17.051.03.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Heidbrink Helmut Zepf root tip pick?
The Heidbrink root tip pick, referenced under code 17.051.03, is a specialized manual instrument designed by Helmut Zepf Medizintechnik GmbH. This device is specifically developed for the manipulation and removal of small elements during surgical interventions. Its structure is composed of medical grade stainless steel, ensuring resistance adapted to the constraints of oral surgery. As a fragment extractor, it allows access to narrow areas of the socket to mobilize root structures or bone debris. This product belongs to the category of consumables reusable after a strict sterilization protocol.
What are the clinical indications for this instrument?
This Heidbrink root tip pick is indicated for the extraction of fragments and roots during exodontia or implant surgery procedures. Its primary use lies in the clearing and recovery of fractured root debris or small bone fragments (splinters) that could hinder healing or subsequent implant placement. The Helmut Zepf root fragment instrument is particularly useful when conventional extraction instruments, such as forceps or standard elevators, do not allow a sufficient grip on small structures located deep within the periodontium.
What are the technical characteristics of device 17.051.03?
The Helmut Zepf model 17.051.03 is characterized by its manufacture in medical stainless steel, a material chosen for its biocompatibility and its ability to undergo repeated reprocessing cycles. It is a manual instrument non-sterile upon delivery, requiring rigorous preparation before each use. Its design is optimized for gripping fine fragments, offering the practitioner the tactile control necessary during delicate root picking maneuvers. The manufacturer does not define a maximum limit for usage cycles, as this depends on maintenance and the absence of visible damage such as cracks or defects on the active parts.
What are the contraindications for the use of this fragment extractor?
The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. As the instrument is made of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and the necessary clinical measures must be taken. Apart from this material-related contraindication, use is reserved exclusively for qualified healthcare professionals mastering dental surgery techniques.
What are the maintenance and sterilization precautions?
The Heidbrink root tip pick is delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. Helmut Zepf emphasizes the critical importance of cleaning each product before exposing it to a sterilization cycle. The practitioner must inspect the instrument for any visible damage, such as cracks, breaks, or wear on the cutting edges. It is strictly forbidden to use a damaged product. Although no cycle limit is set, the longevity of the device depends on compliance with reprocessing protocols and prior verification of compatibility with other products used simultaneously.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (Class Ir according to the technical nomenclature mentioned). The manufacturer guarantees that the product meets the safety and performance requirements for a manual dental instrument. As a Class I device, it follows European regulations relating to medical devices (MDR). Maintaining compliance relies on a strict cleaning and sterilization protocol under the responsibility of the healthcare professional, in accordance with the instructions provided by Helmut Zepf to ensure patient safety and instrument efficacy.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
| Tags | |
|---|---|
| Tags | |