SEMKEN-TAYLOR straight tweezers - Helmut Zepf (22.278.15) - Delynov
The Précelle mors droite SEMKEN-TAYLOR - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 22.278.15.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the SEMKEN-TAYLOR straight jaw dressing forceps?
The SEMKEN-TAYLOR straight jaw dressing forceps, referenced under code 22.278.15 at Delynov, is a high-precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this Semken forceps features a straight structure adapted to the requirements of micro-surgery and oral surgery. It is specifically developed to provide a reliable interface between the practitioner's hand and the tissues or materials manipulated at the operative site. This device belongs to the category of reusable consumables, requiring a complete reprocessing cycle before each use to ensure patient safety and instrument longevity.
What are the clinical indications for this instrument?
The intended use of this Helmut Zepf instrument covers several critical needs in surgery. It is indicated for surgically holding or grasping soft tissues, thus allowing for optimal exposure of the operative field or stabilization during suturing. Beyond tissue manipulation, this forceps is used to remove foreign bodies, handle swabs, or manage suture threads during surgery. Its Taylor design allows for fine gripping, essential in implantology or periodontology procedures where the delicacy of anatomical structures requires the use of perfectly calibrated tools for a secure movement.
What are the technical characteristics of reference 22.278.15?
The SEMKEN-TAYLOR forceps is distinguished by its straight jaws and its manufacture from high-quality medical stainless steel. This material is chosen for its resistance to repeated decontamination and sterilization cycles. As a Class I device, it meets the regulatory safety requirements for non-invasive or surgically invasive instruments for temporary use. The ergonomic design specific to Helmut Zepf ensures precise force transmission without excessive fatigue for the surgeon. It is important to note that the product is delivered non-sterile and must imperatively undergo cleaning and sterilization before its first use, in accordance with the manufacturer's instructions.
What are the contraindications for the use of this forceps?
The main medical contraindication identified concerns patients with a known hypersensitivity or intolerance to metals, and more specifically to the components of medical stainless steel. In the event of a hypersensitivity reaction triggered during contact with the instrument during the intervention, the manufacturer Helmut Zepf specifies that the procedure must be immediately stopped in order to take the necessary clinical measures. It is therefore recommended to check the patient's allergic history before any manipulation. Furthermore, the use of an instrument showing visible damage, such as cracks, breaks, or defects on the gripping areas, is strictly prohibited to avoid any risk of complication.
What are the maintenance and reprocessing precautions?
As it is a non-absorbable and reusable instrument, maintenance is crucial. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The practitioner must visually inspect the device to detect any signs of wear or corrosion. Due to the robust design and materials used, there is no defined maximum limit for treatment cycles, as long as the functional integrity of the forceps is preserved. Strict compliance with cleaning protocols guarantees not only asepsis but also compatibility with other instruments used during complex surgical trays.
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 recognized manufacturer in the dental sector ensures the compliance of its products with European safety standards. The SEMKEN-TAYLOR forceps is classified as a Class I medical device according to current regulations. The use of this instrument is strictly reserved for qualified healthcare professionals. Each stage of production, from the choice of steel to the finishing of the jaws, is controlled to meet the requirements of the MDR (Medical Device Regulation), thus ensuring the traceability and reliability essential in a surgical environment.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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