Removable Figure 210-S Dental Form - Helmut Zepf (14.210.05) - Delynov

What is the Helmut Zepf extraction forceps figure 210-S?

The Helmut Zepf extraction forceps figure 210-S, bearing the technical reference 14.210.05, is a manual dental instrument specifically designed for extraction procedures. Manufactured from high-quality medical stainless steel, this device belongs to the category of removable form instruments. Its structure is designed to meet the requirements of oral surgery, providing a robust interface between the practitioner's hand and the intervention area. As a Class I device, it meets the rigorous manufacturing standards of Helmut Zepf Medizintechnik GmbH, guaranteeing a reliable tool for daily avulsion procedures in dental offices or hospital settings.

What are the clinical indications for this instrument?

The primary indication for this Helmut Zepf forceps is its use as a manual dental instrument during extractions. It is intended for dental surgeons and implantologists to facilitate the removal of dental elements. Its use is strictly reserved for qualified healthcare professionals. The device is used within various surgical protocols where a controlled gripping force is required. According to the manufacturer's data, the instrument must be used exclusively for its intended purpose, namely mechanical manipulation during invasive dental care, while respecting pre-operative hygiene and sterilization protocols.

What are the technical characteristics of the 14.210.05 forceps?

This forceps is distinguished by its manufacture in medical stainless steel, a material chosen for its resistance to repeated sterilization cycles. Referenced under code 14.210.05, it features a so-called "figure 210-S" configuration. The manufacturer specifies that due to the product design and the materials used, there is no defined maximum limit for the number of feasible processing cycles, although the user must check for the absence of visible damage before each use. The instrument is delivered non-sterile and requires a complete protocol of cleaning, disinfection, and sterilization before its first use as well as between each patient to ensure clinical safety.

What are the contraindications for the use of this device?

The main medical contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns hypersensitivity to metals. Contact with medical stainless steel can cause an intolerance or hypersensitivity reaction in certain sensitive patients. If such a reaction occurs during the intervention, the procedure must be immediately stopped and the necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before use. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the cutting edges, as this could compromise the safety of the care.

What are the maintenance and sterilization precautions?

As the Helmut Zepf forceps is delivered non-sterile, it is mandatory to perform complete cleaning, disinfection, and sterilization before the first use. This procedure must be repeated after each subsequent use. The manufacturer emphasizes the importance of cleaning each product before use and inspecting the instrument to detect any visible wear. The use of damaged or worn products is strictly prohibited. Although no limit on reprocessing cycles is set, the longevity of the device depends on strict compliance with maintenance instructions. Compatibility with other products used during surgery must also be verified beforehand by the practitioner.

Who is the manufacturer and what standards are respected?

This medical device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I instrument, compliant with regulatory requirements for manual medical devices. As a recognized manufacturer, Helmut Zepf ensures the traceability and quality of its instruments through controlled manufacturing processes. The product is identified by reference 14.210.05 and is intended exclusively for professional use by healthcare experts. Compliance with the instructions provided by the manufacturer regarding reprocessing and visual inspection is essential to maintain the device's conformity throughout its operational life.

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Surgical medical consumables play a decisive role in operative safety.