Skip to Content

Curette Tip - Helmut Zepf (24.751.107GM5) - Delynov

https://www.delynov.fr/web/image/product.template/9623/image_1920?unique=38aaa7a

The Pointe de curette - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.751.107GM5.
  • Reserved for healthcare professionals. Read instructions carefully before use.

31.60 € 31.6 EUR 31.60 € Tax Included

31.60 € Tax Included

(31.60 € / Units)
  • Manufacturer

This combination does not exist.

Instrument

What is the Helmut Zepf curette tip?

The Helmut Zepf curette tip, referenced under code 24.751.107GM5, is a specific manual instrument intended for odontological use. Manufactured by Helmut Zepf Medizintechnik GmbH, it is designed in high-quality medical stainless steel to guarantee resistance to repeated reprocessing cycles. As a Class I instrument, it meets the basic regulatory requirements for non-invasive or temporary invasive devices. Its structure is optimized to allow precise access to complex anatomical areas during periodontal or surgical care, thus offering a response adapted to the needs of oral surgery practitioners.

What are the clinical indications for this instrument?

This instrument is indicated as a manual dental instrument for various procedures in dental offices and operating rooms. It is primarily used in periodontology for subgingival scaling and root planing, allowing for the removal of calcified deposits and infected tissue. In implant or oral surgery, the Helmut Zepf curette tip can be used for cleaning post-extraction sockets or removing inflammatory tissue. Its use is strictly reserved for qualified healthcare professionals, ensuring safe and effective handling within the framework of periodontal treatments and preparatory phases for implantation.

What are the technical characteristics of the 24.751.107GM5 tip?

The Helmut Zepf curette tip is distinguished by its medical stainless steel composition, a material chosen for its biocompatibility and durability. The manufacturer, Helmut Zepf Medizintechnik GmbH, delivers this product non-sterile, which requires a complete cycle of cleaning, disinfection, and sterilization before the first use as well as between each patient. The technical design of reference 24.751.107GM5 allows for precise integration onto compatible handles of the brand. It is imperative to check for the absence of visible damage, such as cracks or wear of the cutting edges, before any intervention to maintain the operational efficiency of the instrument.

What are the contraindications for the use of this instrument?

The main contraindication related to the use of this medical stainless steel instrument is the patient's known hypersensitivity or intolerance to metals. An allergic reaction may be triggered during contact between the instrument and mucosal or bone tissues. If such a hypersensitivity reaction occurs during the intervention, the manufacturer Helmut Zepf specifies that the procedure must be immediately interrupted and necessary medical measures must be taken. It is the practitioner's responsibility to check the patient's allergic history before any use of this manual instrument.

What are the maintenance and reprocessing precautions?

As Helmut Zepf products are delivered non-sterile, they must imperatively undergo cleaning, disinfection, and sterilization before each use. Reprocessing must be carried out according to current hospital protocols. Due to the design of the instrument and the materials used, there is no defined maximum limit for treatment cycles, as long as the instrument does not show signs of degradation. The practitioner must carefully inspect the tip to detect any trace of corrosion, breakage, or defects on the sharp edges. The use of a damaged or worn instrument is prohibited to guarantee patient safety and the effectiveness of the surgical procedure.

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 medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its production processes to meet the requirements of healthcare professionals. Traceability is ensured by the technical reference 24.751.107GM5. As a Class I device, it complies with the safety and performance standards applicable to manual stainless steel instruments intended for dental surgery, thus guaranteeing constant reliability during clinical interventions.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
Tags
Tags
Instrument