Points for Miller - Helmut Zepf (19.272.02) - Delynov

What is the Helmut Zepf Miller tip (19.272.02)?

The Miller tip, referenced under code 19.272.02, is a replacement component designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is manufactured from medical grade stainless steel, ensuring compatibility with rigorous in-office sterilization protocols. As a dental instrument spare part, it maintains the operational efficiency of hand instruments used in oral surgery without requiring the complete replacement of the instrument handle or body. Its design meets the precision requirements necessary for delicate interventions on periodontal or alveolar tissues.

What are the clinical indications for this accessory?

This Miller tip is indicated as a manual dental instrument for various oral surgery procedures. It is primarily used as a syndesmotome replacement part or for light luxation maneuvers and separation of epithelial-connective attachments before an extraction or implant placement. Its use is strictly reserved for qualified healthcare professionals. It is integrated into implant and periodontal surgery protocols where precise manipulation of anatomical structures is required. The practitioner must verify the compatibility of this tip with their existing instruments before any clinical intervention.

What are the technical characteristics of reference 19.272.02?

Technical reference 19.272.02 corresponds to a specific tip developed by Helmut Zepf. It is designed in medical stainless steel, a material chosen for its resistance to repeated cleaning and disinfection cycles. This device is delivered non-sterile and must undergo complete processing (cleaning, disinfection, and sterilization) before its first use and after each subsequent use. Due to its design and the materials used, there is no defined maximum limit for processing cycles, but a visual inspection is mandatory to detect any signs of wear, cracks, or defects on the cutting edges before each procedure.

What are the contraindications for the use of this device?

The main medical contraindication lies in the patient's known hypersensitivity or intolerance to metals, particularly the medical stainless steel used in the composition of the instrument. A hypersensitivity reaction may be triggered during direct contact with tissues. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf specifies that the intervention must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to question the patient about their allergic history before using this dental surgery accessory.

What are the maintenance and safety precautions?

Reprocessing the Miller tip 19.272.02 is a critical step for patient safety. All Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. The protocol requires cleaning, disinfection, and sterilization before the first use. Before each use, the practitioner must perform a thorough visual check to identify potential damage such as cracks, breaks, or wear on the active parts. It is strictly forbidden to use a damaged product. Furthermore, compatibility with other instruments in the range must be verified beforehand to ensure secure assembly during the surgical act.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. The product is classified as a Class I medical device according to current regulations. The manufacturer complies with safety and performance requirements for manual dental instruments. As a Class I device, it meets German manufacturing quality standards for stainless steel instruments. Traceability is ensured by reference 19.272.02, allowing dental surgery practices to precisely manage their spare parts inventory and ensure the monitoring of used medical devices.

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