ZEPF-BIONIK. BOUCHON D'IDENTIFICATION. - Helmut Zepf

What is the ZEPF-BIONIK IDENTIFICATION PLUG?

The ZEPF-BIONIK is an identification plug designed by Helmut Zepf Medizintechnik GmbH to be fixed onto manual instrumentation. This component belongs to the category of consumables for practice organization. Its structure is specifically adapted to fit the handles of instruments in the Bionik range, thus allowing tools to be differentiated by a simple visual system. It meets the needs for clarity in stock and technical tray management, preventing confusion between instruments with similar morphologies during clinical procedures.

What are the clinical indications for this instrument color plug?

In oral, periodontal, or implant surgery, the use of this instrument color plug allows instrumentation to be segmented by procedure type or by practitioner. It is indicated for marking curettes, periosteal elevators, or needle holders within a hospital department or private practice. By facilitating immediate identification, it optimizes the workflow during complex interventions where rapid access to the appropriate instrument is necessary. This device participates in the standardization of sterile tray preparation protocols.

What are the technical characteristics of model 26.195.10?

The product bears the technical reference 26.195.10 in the Helmut Zepf catalog. It is presented as a removable dental identification ring, designed to withstand repeated cleaning and disinfection cycles. Although precise material specifications are not detailed in the source data, this type of accessory is generally developed to withstand the thermal stresses associated with the maintenance of surgical equipment. Its design allows for stable fixation on the handle without compromising the grip of the instrument by the dental surgeon or assistant.

What are the contraindications for the use of this device?

There are no specific documented medical contraindications for the external use of this identification plug on instrumentation. However, it should be ensured that the plug is correctly positioned and shows no signs of degradation (cracks or loss of elasticity) that could compromise hygiene or safety during handling. Its use is strictly reserved for equipment identification and it must under no circumstances come into direct contact with the patient's tissues during the surgical procedure.

What precautions should be taken for maintenance and sterilization?

As an autoclave identification ring, this plug must be processed in accordance with the sterilization protocols in force for the instrumentation it equips. It is recommended to check the compatibility of the instrumentation color code with the chemical cleaning agents used to avoid any premature discoloration. The practitioner must ensure that no organic residue is trapped between the plug and the instrument handle. A visual check after each sterilization cycle is recommended to guarantee the integrity of the device and the maintenance of its fixation properties.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a company recognized for manufacturing high-precision surgical instruments. Regarding standards and certifications, the regulatory class and specific CE marking are not specified in the provided technical documentation. Users are invited to refer to the instructions for use and the technical manual from the manufacturer Helmut Zepf to obtain details relating to conformity certifications and exact recommendations for thermal or chemical reprocessing of the product.

State of the art

Surgical medical consumables play a decisive role in operative safety.