Micro-Halstead Hemostatic Forceps for Dental Surgery and Implantology - Helmut Zepf (23.063.12) - Delynov

What is the Helmut Zepf micro-Halstead hemostatic forceps?

The micro-Halstead hemostatic forceps (reference 23.063.12) is a manual instrument designed by Helmut Zepf Medizintechnik GmbH for high-precision interventions. Manufactured from medical stainless steel, this dental micro halstead forceps is distinguished by its fine structure adapted to restricted surgical environments. It belongs to the category of GBR and oral surgery instruments, offering a reliable solution for the secure grasping and holding of tissues or vessels. Its robust stainless steel design ensures the necessary resistance to repeated sterilization cycles in the dental office.

What are the clinical indications in oral surgery?

This oral surgery hemostatic forceps is primarily indicated for achieving hemostasis by compressing blood vessels to interrupt bleeding during an intervention. In implantology, it is used for manipulating membranes or soft tissues during bone grafts (GBR). The precision hemostatic forceps also allows for grasping small fragments or foreign bodies with great safety. Its use is strictly reserved for qualified healthcare professionals practicing dental surgery, implantology, or periodontology, requiring an instrument capable of maintaining constant pressure without excessively traumatizing surrounding tissues.

What are the technical characteristics of this instrument?

The micro halstead forceps, referenced under code 23.063.12, is a Class I device according to medical device regulations. It is designed by Helmut Zepf with a specific geometry allowing access to posterior or difficult-to-reach areas of the oral cavity. As a manual instrument, it does not include an integrated needle. Its medical stainless steel construction provides standard biocompatibility, although the practitioner must remain vigilant regarding hypersensitivity risks. The locking mechanism allows for adjustable and maintained gripping force, essential for long-duration procedures in oral surgery.

What are the contraindications for the use of these forceps?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns intolerance or allergy to metals. If a patient exhibits a hypersensitivity reaction upon contact with the medical stainless steel of the instrument, the procedure must be immediately stopped and necessary clinical measures must be taken. It is the practitioner's responsibility to check the patient's allergic history before any surgical intervention. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as cracks, breaks, or defects on the active parts.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is crucial to inspect the implantology hemostatic forceps before each intervention to detect any signs of wear or corrosion. Due to its design and the materials used, there is no defined maximum limit for processing cycles, but the instrument must be discarded as soon as defects appear on the cutting edges or the closing mechanism. Strict compliance with reprocessing protocols guarantees patient safety and the longevity of the tool.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is listed as Class I (Class Ir according to certain reprocessing nomenclatures). It meets the quality requirements for medical stainless steel for prolonged surgical use. The manufacturer requires that compatibility with other products used during the intervention be verified beforehand. As a precision instrument, it follows the rigorous German industry manufacturing standards for manual medical devices intended for dental and oral surgery.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.