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Halstead-Mosquito 12.5 cm - Helmut Zepf (23.058.12)

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The halstead-mosquito 12,5 cm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 23.058.12.
  • Reserved for healthcare professionals. Read instructions carefully before use.

68.34 € 68.34 EUR 68.34 € Tax Included

68.34 € Tax Included

(68.34 € / Units)
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Instrument

What is the halstead-mosquito 12.5 cm forceps?

The halstead-mosquito 12.5 cm forceps, referenced under code 23.058.12 by Helmut Zepf, is a manual instrument used primarily as surgical hemostatic forceps. Designed by Helmut Zepf Medizintechnik GmbH, it is manufactured from high-quality medical stainless steel to meet the requirements of oral surgery. Its fine structure and 12.5 cm length allow for precise manipulation in restricted access areas of the oral cavity. This device is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient, in accordance with the manufacturer's guidelines.

What are the clinical indications?

In dental and implant surgery, the halstead-mosquito forceps are indicated for soft tissue hemostasis. Their primary role consists of clamping small blood vessels to interrupt the hemorrhagic flow during the surgical act. They are also employed for grasping and holding delicate tissues or small elements during periodontal surgeries, connective tissue graft harvesting, or implant site preparation. Its design allows for secure gripping without excessively damaging surrounding structures, thus facilitating the practitioner's work in complex clinical environments.

What are the technical characteristics?

These Helmut Zepf surgical hemostatic forceps have a total length of 12.5 cm, which classifies them among the mosquito-type instruments, recognized for their fineness. They are manufactured from a medical stainless steel selected for its resistance to repeated sterilization cycles. The ratchet locking mechanism allows for maintaining constant pressure once the forceps are closed on the vessel or tissue. The technical reference 23.058.12 guarantees precise correspondence with the manufacturing standards of Helmut Zepf Medizintechnik GmbH. As a Class I device, it meets the safety and performance requirements for manual dental instruments.

What are the contraindications for use?

The main documented medical contraindication for this instrument is known hypersensitivity or intolerance to metals in the patient. As the instrument is composed of medical stainless steel, contact may trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is strictly reserved for qualified healthcare professionals. It is also contraindicated to use the product if it shows visible damage such as cracks, breaks, or defects on the edges, as this could compromise patient safety and the effectiveness of the surgical gesture.

What are the maintenance and reprocessing precautions?

The reprocessing of the Helmut Zepf halstead-mosquito forceps follows a strict protocol since the device is delivered non-sterile. Before the first use and after each subsequent use, the instrument must undergo a complete cycle including cleaning, disinfection, and sterilization. The manufacturer specifies that it is imperative to check for the absence of visible damage and wear, notably cracks or ruptures, before any implementation. Due to the robust design and materials used, there is no defined maximum limit of treatment cycles, as long as the physical integrity of the instrument is preserved. Compatibility with other cleaning and sterilization products must be verified beforehand by the professional.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures) in accordance with current regulations. Helmut Zepf is a recognized manufacturer in the field of dental instrumentation, ensuring traceability and manufacturing quality compliant with medical sector requirements. The instrument must be used in accordance with its intended purpose as a manual dental instrument. Compliance with the instructions for use and safety provided by Helmut Zepf is essential to guarantee the longevity of the tool and the safety of the care provided in a practice or hospital environment.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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