Special Handle Elevator - Helmut Zepf (17.101.61) - Delynov

What is the Helmut Zepf special elevator (17.101.61)?

The Helmut Zepf special elevator, referenced under code 17.101.61, is a precision manual instrument intended for oral surgery. Its structure consists of an active working part and a specific wide handle designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this tool is designed to withstand mechanical stress during extractions. It belongs to the Class I instrument category according to medical device regulations. Its robust design ensures efficient force transmission during leverage maneuvers, while respecting German manufacturing quality standards.

What are the clinical indications for this wide handle dental elevator?

This wide handle dental elevator is primarily indicated for the luxation of teeth and residual roots. In dental and implant surgery, it is used to widen the socket and break the ligament attachment before extraction. Its use is reserved for qualified healthcare professionals practicing oral surgery procedures. The instrument allows access to interproximal spaces to mobilize the dental structure with control. It is particularly useful in cases where direct grip with forceps is impossible or risky without prior mobilization of the root.

What are the technical characteristics of this instrument?

The Helmut Zepf 17.101.61 instrument is distinguished by its ergonomic wide handle which optimizes practitioner comfort during repetitive procedures. Manufactured from high-quality medical stainless steel, it is delivered non-sterile and requires a rigorous preparation protocol before each use. This Class I device is designed to be durable, although it does not have a defined maximum limit for processing cycles, provided the integrity of the steel is preserved. Every professional must check for the absence of visible damage, such as cracks or defects on the edges, before any clinical intervention.

What are the contraindications for the use of this elevator?

The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the surgical act, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore crucial to validate the absence of metal allergies during the patient's preoperative anamnesis.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use as well as after each subsequent use. Reprocessing must be complete to ensure patient safety and the longevity of the stainless steel. It is imperative to clean each product individually and visually inspect the instrument to detect any trace of wear, corrosion, or deformation. The use of damaged products or those presenting defective cutting edges is strictly prohibited. Compatibility with other cleaning and disinfection products must also be verified beforehand by the healthcare staff.

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 certain reprocessing nomenclatures). As a high-precision manual instrument, it meets the manufacturing requirements for medical stainless steel. The manufacturer emphasizes that its products are reserved exclusively for healthcare professionals. Compliance with cleaning and sterilization protocols is essential to maintain the conformity of the device throughout its useful life in a dental office or hospital environment.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.