English pattern dental extraction forceps, Figure 36M - Helmut Zepf (12.236.08ZD) - Delynov

What is the Helmut Zepf Figure 36M extraction forceps?

The Figure 36M extraction forceps, referenced under code 12.236.08ZD by Helmut Zepf, is a manual instrument specific to oral surgery. Manufactured from medical stainless steel, this English pattern device is designed to meet gripping requirements during extractions. As a Class I instrument, it is part of the range of manual diagnostic and treatment tools from the manufacturer Helmut Zepf Medizintechnik GmbH. Its robust structure ensures adequate force transmission while respecting the material quality standards required for invasive interventions in a clinical setting.

What are the clinical indications for this instrument?

This extraction forceps is indicated for manual dental extraction. Its use is strictly reserved for qualified healthcare professionals. It is primarily used in oral surgery protocols requiring the avulsion of teeth or roots. The instrument allows the practitioner to firmly grasp the dental element to perform the necessary luxation and extraction movements. Its application must always be preceded by a verification of the instrument's integrity to ensure the absence of visible damage such as cracks or defects on the active parts.

What are the technical characteristics of the 12.236.08ZD extraction forceps?

The Helmut Zepf Figure 36M extraction forceps is characterized by its composition of high-quality medical stainless steel. It is a non-sterile instrument upon delivery, requiring a full reprocessing cycle before each use. Its English pattern design is optimized for manual ergonomics in the dental office. Due to the materials used and the robustness of its manufacture, there is no defined maximum limit for treatment cycles (cleaning, disinfection, sterilization), provided that visual examination reveals no wear or structural degradation compromising safety.

What are the contraindications for the use of this device?

The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity to metals. An intolerance reaction may occur in sensitive patients upon contact with the medical stainless steel composing the instrument. If such a hypersensitivity reaction is triggered during the procedure, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, it is formally contraindicated to use the instrument if it shows visible signs of wear, breaks, or defects on the cutting edges.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use, and then after each subsequent use. The cleaning process must be complete to guarantee patient safety and the longevity of the steel. It is crucial to inspect the product before each intervention to detect any visible damage, such as cracks or defects on the beaks. The use of damaged or worn products is prohibited. Reprocessing depends on the product design and the sterilization cycles applied in a hospital or office setting.

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 in accordance with medical device regulations. The manufacturer guarantees the use of compliant medical stainless steel for surgical practice. The products are delivered non-sterile and must be processed according to current disinfection and sterilization protocols. Traceability and compliance with safety requirements are ensured by the rigorous manufacturing processes of Helmut Zepf, a recognized player in dental instrumentation.

State of the art

Surgical medical consumables play a decisive role in operative safety.