English pattern dental extraction forceps, model FIG.36N - Helmut Zepf (12.236.07ZD) - Delynov

What is the Helmut Zepf FIG.36N extraction forcep?

The FIG.36N extraction forcep, referenced under code 12.236.07ZD, is a high-precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. This Class I medical device is designed from medical-grade stainless steel, specifically selected to meet the requirements of oral surgery. Its English pattern structure is optimized to ensure a stable grip and effective transmission of force during avulsion procedures. As a reusable instrument, it requires a strict reprocessing protocol to guarantee patient safety.

What are the clinical indications for this instrument?

This forcep is indicated for manual dental extraction procedures. In dental and oral surgery, it is used by the practitioner to firmly grasp the crown or root of a tooth in order to proceed with its luxation and then its complete extraction. Its use is strictly reserved for qualified healthcare professionals. The manufacturer Helmut Zepf specifies that the instrument must be inspected before each use to detect any visible damage, such as cracks or defects on the active parts, to ensure the integrity of the surgical act.

What are the technical characteristics of the 12.236.07ZD forcep?

The Helmut Zepf model FIG.36N forcep is distinguished by its manufacture in medical stainless steel, a material recognized for its resistance to corrosion and durability through repeated sterilization cycles. This English pattern model is delivered non-sterile and must imperatively undergo cleaning, disinfection, and sterilization before the first use, as well as between each patient. Its ergonomic design allows for precise handling, although the manufacturer does not define a maximum limit for treatment cycles, as this depends on actual wear and the care taken during reprocessing.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. Contact of the medical stainless steel instrument with an allergic patient may trigger a hypersensitivity reaction. If such a reaction occurs during the procedure, the intervention must be immediately interrupted and necessary medical measures must be taken. It is therefore crucial to assess the patient's allergic history before using this manual instrument in the mouth.

What are the maintenance and safety precautions?

To ensure the safety and longevity of the Helmut Zepf instrument, all devices must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to check for the absence of visible damage, breakage, or pronounced wear before each intervention. The use of damaged products or those presenting defects on the cutting edges is strictly prohibited. Compatibility with other products used during surgery must also be verified beforehand by the healthcare professional.

Who is the manufacturer and what standards are respected?

This forcep is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I medical device compliant with regulatory requirements for manual dental instruments. The manufacturer emphasizes that reprocessing of the instrument is possible thanks to the quality of the materials used, although the service life depends on maintenance and the absence of mechanical damage. As a Class I product, it meets the safety and performance standards required for non-invasive or invasive medical devices for temporary use.

State of the art

Surgical medical consumables play a decisive role in operative safety.