Elevator Root picks - Helmut Zepf (17.195.00) - Delynov

What is the Helmut Zepf Bill Becker root elevator?

The Bill Becker root elevator, bearing reference 17.195.00, is a manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This specialized tool belongs to the category of consumables for oral surgery. It is manufactured from medical stainless steel, a standard material ensuring the rigidity necessary for luxation maneuvers. As an instrument of the Helmut Zepf brand, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation. This device is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use in the office or operating theater.

What are the clinical indications for this root elevator?

The use of this bill becker root elevator is indicated for tooth extraction procedures, particularly when mobilizing deeply anchored or fractured roots. In oral and implant surgery, this root elevator allows for the application of controlled leverage forces to break the periodontal ligament fibers. Its use is reserved for qualified healthcare professionals practicing complex avulsions. The instrument is specifically adapted to facilitate access to narrow areas of the alveolus, thus allowing the root to be cleared without excessive damage to the surrounding bone walls, which is crucial for site preservation in view of future implantation.

What are the technical characteristics of instrument 17.195.00?

The Helmut Zepf instrument reference 17.195.00 is characterized by its high-quality medical stainless steel construction. Although specific dimensions are not detailed, its design meets the requirements of manual dental surgery interventions. It is a curved dental elevator, optimized for ergonomics and force transmission during luxation. The manufacturer emphasizes that the product design and materials used do not allow for the definition of a maximum limit of processing cycles, although the user must imperatively check for the absence of visible damage, such as cracks or defects on the cutting edges, before each intervention.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient can trigger a reaction in allergic individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore recommended to question the patient about their history of metal allergies before any use of this manual instrument in the mouth.

What are the maintenance and reprocessing precautions?

Like any Class I non-sterile instrument, this root elevator requires a strict reprocessing protocol. Before the first use and after each subsequent use, the instrument must be cleaned, disinfected, and sterilized. The practitioner must visually inspect the device to detect any signs of wear, corrosion, or breakage. The use of damaged products or those with defective cutting edges is strictly prohibited to guarantee patient safety and the effectiveness of the surgical gesture. Compatibility with other cleaning and sterilization products must also be verified beforehand by the healthcare staff.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is classified as a Class I device according to current regulations. The manufacturer respects rigorous quality standards for the production of manual dental instruments in medical stainless steel. Although the specific CE marking is not detailed in the source data, the product meets the safety and performance requirements for instruments intended for healthcare professionals. Each unit is identified by the technical reference 17.195.00, ensuring the traceability of the device within the Helmut Zepf range.

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