Removable Figure 222-AS Dental Form - Helmut Zepf (14.222.11) - Delynov

What is the Helmut Zepf 14.222.11 removable form forceps?

The figure 222-AS removable form forceps, bearing reference 14.222.11, is a manual instrument specifically designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this device is intended for the practice of dental and oral surgery. It belongs to the category of reusable consumables (Class I) and is distinguished by its robust structure adapted to the mechanical stresses of extraction. As a non-sterile instrument upon delivery, it requires a complete preparation protocol before its first use in the office or operating room.

What are the clinical indications?

This instrument is indicated as a manual dental instrument for exodontia procedures. It is primarily used by dental surgeons and implantologists for the extraction of teeth or roots. Its use is strictly reserved for qualified healthcare professionals. The forceps allow for a firm grip to facilitate the luxation movement and final avulsion, integrating into standard oral surgery, periodontology, or pre-implant preparation protocols.

What are the technical characteristics?

The figure 222-AS forceps (reference 14.222.11) is manufactured from a medical grade stainless steel selected by Helmut Zepf. This material ensures the necessary resistance to repeated cleaning and sterilization cycles. The device is classified as a Class I instrument according to medical device regulations. Its "removable form" design meets specific gripping needs during extractions. It is delivered in a non-sterile state, requiring validation of the instrument's condition (absence of cracks, breaks, or defects on the edges) before each intervention.

What are the contraindications for use?

The main medical contraindication identified by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance of the patient to metals, particularly to the components of medical stainless steel. If a hypersensitivity reaction is triggered upon contact with the instrument, the procedure must be immediately stopped and necessary medical measures must be taken. Additionally, the use of the instrument is contraindicated if it shows visible damage, such as cracks or excessive wear, as this could compromise the safety of the patient and the practitioner.

What are the maintenance and reprocessing precautions?

As it is a non-sterile and reusable instrument, it is imperative to follow a strict cycle of cleaning, disinfection, and sterilization before the first use and after each subsequent use. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit of processing cycles, as long as the instrument shows no signs of degradation. It is crucial to visually inspect the forceps before each use to detect any trace of wear, breakage, or defect on the active parts. Any damaged product must never be used.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with regulatory requirements relating to medical devices, classifying this forceps as Class I. Although the specific CE marking is not detailed in the source data, the product meets manufacturing standards for manual medical stainless steel instruments. The manufacturer emphasizes that the use of this device is strictly reserved for healthcare professionals and that compatibility with other products must be verified beforehand.

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