PLAQUETTE D'IDENTIFICATION - Helmut Zepf

What is the Helmut Zepf identification plate?

The Helmut Zepf identification plate, bearing reference 85.312.04, is a logistics management accessory designed for the clinical environment. This instrument marking device allows for the differentiation and organization of surgical sets within the practice. Manufactured by Helmut Zepf Medizintechnik GmbH, this identification tag is designed to withstand repeated cleaning and sterilization cycles. It is part of a traceability and surgical tray optimization approach, ensuring immediate visual identification of instruments during the preparation and intervention phases in dental or implant surgery.

What are the clinical indications for this device?

Although the plate itself is not an active operative instrument, it is indicated for the organization of manual dental instruments. Its use is essential in facilities performing varied interventions such as periodontology, implantology, or oral surgery, where the separation of instrument kits is crucial. It helps maintain the consistency of instrument sets throughout the reprocessing chain, from chairside use to final sterilization. This marking helps healthcare personnel quickly identify the function or assignment of each instrument.

What are the technical characteristics of this product?

The Helmut Zepf identification plate (technical reference 85.312.04) is designed to be attached to the brand's instruments. It is manufactured from materials compatible with hospital disinfection and sterilization protocols. This device belongs to the category of consumables (CONSO) and is classified as a Class I medical device according to current regulations. Its design allows for durable attachment without interfering with the grip or clinical use of the instrument on which it is placed, thus guaranteeing constant safety of use for the practitioner.

What are the contraindications for the use of this marking?

According to data from the manufacturer Helmut Zepf Medizintechnik GmbH, the main contraindication concerns hypersensitivity or intolerance to metals. As the instrument is made of medical stainless steel, direct contact can trigger a reaction in sensitive patients. If such a hypersensitivity reaction occurs during the procedure, the procedure must be stopped immediately and the necessary clinical measures must be taken. It is therefore recommended to check the patient's allergic history before any intervention involving contact with stainless steel devices.

What are the precautions related to maintenance and reprocessing?

Like any instrument in the Helmut Zepf range, this plate must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to inspect the product before any use to detect potential visible damage such as cracks, breaks, or defects. The products are delivered non-sterile and must undergo a complete preparation cycle. Due to its design and the materials used, there is no defined maximum limit for processing cycles, but use must cease upon the appearance of signs of wear or degradation.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product complies with Class I medical device regulations. The manufacturer emphasizes that the use of these products is strictly reserved for qualified healthcare professionals. Compliance with cleaning and sterilization protocols is the responsibility of the practitioner, in accordance with the instructions provided by Helmut Zepf to ensure patient safety and the longevity of the instrument marking equipment.

State of the art

Surgical medical consumables play a decisive role in operative safety.