Hemingway Modifie Surgical Kit - Helmut Zepf (41.846.11) by Delynov
The hemingway modifie - helmut zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 41.846.11.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf modified Hemingway?
The modified Hemingway, referenced under code 41.846.11, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device belongs to the category of reusable consumables for oral surgery. Its structure is entirely made of medical stainless steel, a standard material ensuring the rigidity necessary for clinical interventions. As a hand instrument, it is intended to be handled by healthcare professionals for precise movements within the oral cavity. This specific model benefits from Helmut Zepf's expertise in the design of precision tools for dentistry.
What are the clinical indications for this instrument?
The modified Hemingway instrument is primarily indicated for oral and implant surgery procedures. Its intended use, as defined by the manufacturer Helmut Zepf Medizintechnik GmbH, is that of a manual dental instrument. In clinical practice, this type of modified curette or excavator is used for cleaning post-extraction sockets, removing inflammatory tissue or soft tissue debris, as well as for the curettage of periapical lesions. It also allows for the preparation of the bone site before implant placement by ensuring the cleanliness of the alveolar walls. Its application is strictly reserved for qualified healthcare professionals.
What are the technical characteristics of model 41.846.11?
Model 41.846.11 is characterized by its construction from high-quality medical stainless steel. This material is chosen for its mechanical resistance and its ability to withstand repeated thermal and chemical treatment cycles. The instrument is delivered in a non-sterile state, which requires a strict preparation protocol before the first use and between each patient. The design of the modified Hemingway instrument by Helmut Zepf does not specify a defined maximum limit for treatment cycles, as the lifespan depends on visible wear and the integrity of the active parts of the instrument during reprocessing.
What are the contraindications for the use of this instrument?
The main medical contraindication documented by the manufacturer Helmut Zepf concerns known hypersensitivity or intolerance to metals. As the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and necessary clinical measures must be taken. It is therefore recommended to question the patient about their history of metal allergies before any use of this manual instrument in the mouth.
What are the maintenance and sterilization precautions?
All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before their first use and after each subsequent use. Before each use, the practitioner must perform a thorough visual inspection to detect potential damage or signs of wear, such as cracks, breaks, or defects on the cutting edges. It is strictly forbidden to use a damaged or worn product. The reprocessing process must be complete to ensure patient safety and the longevity of the stainless steel. Compatibility with other cleaning and disinfection products must also be verified beforehand by the professional.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I (more specifically Class Ir according to reprocessing mentions). As a recognized manufacturer in the dental sector, Helmut Zepf ensures the traceability and quality of its products in accordance with the regulatory requirements applicable to manual instruments. Healthcare professionals must refer to the instructions provided by Helmut Zepf Medizintechnik GmbH to ensure use in accordance with the intended purpose and to maintain the safety standards required in a surgical environment.
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Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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