Onyx cheek and lip retractor for oral and dental surgery - Helmut Zepf (37.454.00TI) - Delynov
The Écarteur de joues et de lèvres Onyx pour chirurgie orale et dentaire - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 37.454.00TI.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Onyx retractor (37.454.00TI)?
The Onyx cheek and lip retractor, referenced under code 37.454.00TI, is a specialized instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH for oral and dental surgery. This device is manufactured from medical stainless steel, a material chosen for its robustness and its ability to withstand repeated sterilization cycles. As a holding instrument, it allows the practitioner to effectively retract soft tissues in order to optimize visibility and access to the surgical site. This product is part of the high-quality range from the recognized manufacturer Helmut Zepf, guaranteeing a reliable tool for daily interventions in dental offices or hospital environments.
What are the clinical indications for this buccal retractor?
The intended use of this instrument is strictly defined by the manufacturer for the maintenance of the tongue, lip, cheek, and gingiva. In oral and implant surgery, the use of a lip retractor or labial retractor is essential to clear the field of vision during implant placement, periodontal surgeries, or complex extractions. It allows for the secure stabilization of soft tissues, thereby avoiding visual obstructions and facilitating the passage of rotary or manual instrumentation. Its application is reserved exclusively for qualified healthcare professionals mastering tissue retraction techniques.
What are the technical characteristics of the Onyx retractor?
The Onyx retractor (37.454.00TI) is distinguished by its design in high-quality medical stainless steel. Although delivered non-sterile, it is designed to undergo a complete cleaning, disinfection, and sterilization process before each use. Due to its metallic structure and the materials used, Helmut Zepf specifies that there is no defined maximum limit for the number of reprocessing cycles, as long as the instrument does not show visible damage. The practitioner must imperatively inspect the tool before each use to detect any cracks, breaks, or defects on the edges, in order to guarantee patient safety and the effectiveness of the surgical maneuver.
What are the contraindications for the use of this instrument?
The main contraindication related to the use of this medical stainless steel retractor is hypersensitivity or metal intolerance in the patient. Contact of the instrument with mucous membranes can trigger an allergic reaction in sensitive subjects. According to warnings from the manufacturer Helmut Zepf Medizintechnik GmbH, if a hypersensitivity reaction is observed during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore recommended to question the patient about their history of metal allergies before any manipulation of the instrument in the mouth.
What are the maintenance and sterilization precautions?
To guarantee the longevity and safety of the retractor, all instruments must be cleaned, disinfected, and sterilized before the first use, and then after each subsequent use. It is essential to perform a complete cleaning to remove any biological residue before the sterilization phase. The manufacturer emphasizes that damaged or worn products, showing for example cracks or structural defects, should never be used. Verification of compatibility with other products used simultaneously is also required. Reprocessing is possible without a predefined limit of cycles, subject to the good functional and aesthetic condition of the stainless steel.
Who is the manufacturer and what standards are respected?
This retractor is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. As a Class I product, it meets the safety and performance requirements imposed for non-invasive or temporary invasive reusable surgical instruments. The reliability of the Helmut Zepf brand ensures that dental surgeons benefit from rigorous compliance with manufacturing protocols. It is reminded that the use of this instrument is strictly reserved for healthcare professionals and must comply with the instructions provided by the manufacturer to ensure safe and effective use.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Helmut Zepf |
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